Variant Details

Variant: esv3306941

Internal ID

15153889

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr13:32132250..32132251	hg38	UCSC Ensembl
Inner	chr13:32132233..32132268	hg38	UCSC Ensembl
Outer	chr13:32132232..32132269	hg38	UCSC Ensembl
	chr13:32706387..32706388	hg19	UCSC Ensembl
Inner	chr13:32706370..32706405	hg19	UCSC Ensembl
Outer	chr13:32706369..32706406	hg19	UCSC Ensembl
	chr13:31604387..31604388	hg18	UCSC Ensembl
Inner	chr13:31604405..31604370	hg18	UCSC Ensembl
Outer	chr13:31604369..31604406	hg18	UCSC Ensembl

Cytoband

13q13.1

Allele length

Assembly	Allele length
hg38	293
hg19	293
hg18	293

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7796430, essv7780166, essv7805200, essv7828913, essv7783657, essv7773230, essv7789398, essv7816798, essv7803830, essv7826676, essv7791166, essv7793503, essv7807671, essv7783917, essv7781484, essv7773136, essv7831025, essv7832177, essv7777733, essv7835954, essv7812699, essv7791712, essv7822556, essv7823780, essv7815582, essv7833750, essv7785806, essv7830473, essv7795133, essv7780595, essv7786983, essv7777062, essv7818006, essv7798348, essv7776632, essv7796277, essv7829174, essv7814629, essv7809922, essv7829808

Samples

NA18592, NA12814, NA18980, NA18561, NA11920, NA18526, NA12155, NA18944, NA18940, NA18550, NA12891, NA18547, NA18960, NA18582, NA18571, NA19138, NA18964, NA12156, NA18973, NA18638, NA18951, NA12872, NA18579, NA18572, NA19114, NA18499, NA19225, NA18570, NA18593, NA18542, NA18909, NA19108, NA18961, NA19143, NA19093, NA18609, NA18552, NA12006, NA18562, NA18965

Known Genes

FRY

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3306941

Frequency

Sample Size	185
Observed Gain	40
Observed Loss	0
Observed Complex	0
Frequency	n/a