A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15212047



Internal ID2768445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34904579..34905704hg38UCSC Ensembl
Innerchr15:34904579..34905704hg38UCSC Ensembl
Outerchr15:34904394..34905783hg38UCSC Ensembl
chr15:35196780..35197905hg19UCSC Ensembl
Innerchr15:35196780..35197905hg19UCSC Ensembl
Outerchr15:35196595..35197984hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636126
Supporting Variants
SamplesHG02439
Known GenesAQR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15212047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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