A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638037



Internal ID6678135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15576113..15580633hg38UCSC Ensembl
Innerchr16:15576163..15580583hg38UCSC Ensembl
Outerchr16:15576063..15580683hg38UCSC Ensembl
chr16:15669970..15674490hg19UCSC Ensembl
Innerchr16:15670020..15674440hg19UCSC Ensembl
Outerchr16:15669920..15674540hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg384521
hg194521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385630, essv15385633, essv15385631, essv15385632
SamplesHG02088, NA19010, HG01866, NA18567
Known GenesC16orf45
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638037
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer