A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15439426



Internal ID1970412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27554137..27559858hg38UCSC Ensembl
Innerchr16:27554137..27559858hg38UCSC Ensembl
Outerchr16:27554056..27559964hg38UCSC Ensembl
chr16:27565458..27571179hg19UCSC Ensembl
Innerchr16:27565458..27571179hg19UCSC Ensembl
Outerchr16:27565377..27571285hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385722
hg195722
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638326
Supporting Variants
SamplesHG01817
Known GenesKIAA0556
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15439426
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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