A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15305123



Internal ID1926983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79924445..79953164hg38UCSC Ensembl
Innerchr15:79924945..79952664hg38UCSC Ensembl
Outerchr15:79923445..79954164hg38UCSC Ensembl
chr15:80216787..80245506hg19UCSC Ensembl
Innerchr15:80217287..80245006hg19UCSC Ensembl
Outerchr15:80215787..80246506hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3828720
hg1928720
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637012
Supporting Variants
SamplesHG01799
Known GenesC15orf37
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15305123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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