A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15275361



Internal ID6226278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67287529..67290752hg38UCSC Ensembl
Innerchr15:67287529..67290752hg38UCSC Ensembl
Outerchr15:67287143..67291056hg38UCSC Ensembl
chr15:67579867..67583090hg19UCSC Ensembl
Innerchr15:67579867..67583090hg19UCSC Ensembl
Outerchr15:67579481..67583394hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383224
hg193224
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636778
Supporting Variants
SamplesNA19752
Known GenesIQCH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15275361
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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