A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637050



Internal ID7023844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81988121..81989969hg38UCSC Ensembl
Innerchr15:81988138..81989952hg38UCSC Ensembl
Outerchr15:81988104..81989986hg38UCSC Ensembl
chr15:82280462..82282310hg19UCSC Ensembl
Innerchr15:82280479..82282293hg19UCSC Ensembl
Outerchr15:82280445..82282327hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15307419
SamplesHG03577
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637050
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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