A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271667



Internal ID597591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64780935..64783968hg38UCSC Ensembl
Innerchr15:64780935..64783968hg38UCSC Ensembl
Outerchr15:64780435..64784468hg38UCSC Ensembl
chr15:65073134..65076167hg19UCSC Ensembl
Innerchr15:65073134..65076167hg19UCSC Ensembl
Outerchr15:65072634..65076667hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383034
hg193034
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636744
Supporting Variants
SamplesHG00261
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271667
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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