A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15276117



Internal ID2034069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67391150..67391716hg38UCSC Ensembl
Innerchr15:67391153..67391714hg38UCSC Ensembl
Outerchr15:67391148..67391719hg38UCSC Ensembl
chr15:67683488..67684054hg19UCSC Ensembl
Innerchr15:67683491..67684052hg19UCSC Ensembl
Outerchr15:67683486..67684057hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636786
Supporting Variants
SamplesHG01865
Known GenesIQCH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15276117
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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