A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15373026



Internal ID5374842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10454025..10471134hg38UCSC Ensembl
Innerchr16:10454075..10471084hg38UCSC Ensembl
Outerchr16:10453945..10471214hg38UCSC Ensembl
chr16:10547882..10564991hg19UCSC Ensembl
Innerchr16:10547932..10564941hg19UCSC Ensembl
Outerchr16:10547802..10565071hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817110
hg1917110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637901
Supporting Variants
SamplesNA12830
Known GenesATF7IP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15373026
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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