A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15274164



Internal ID1337040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66623613..66625432hg38UCSC Ensembl
Innerchr15:66623645..66625400hg38UCSC Ensembl
Outerchr15:66623581..66625464hg38UCSC Ensembl
chr15:66915951..66917770hg19UCSC Ensembl
Innerchr15:66915983..66917738hg19UCSC Ensembl
Outerchr15:66915919..66917802hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381820
hg191820
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636770
Supporting Variants
SamplesHG01176
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15274164
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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