A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5756677



Internal ID9679958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74600482..74604108hg38UCSC Ensembl
Outerchr15:74600445..74604158hg38UCSC Ensembl
Innerchr15:74892823..74896449hg19UCSC Ensembl
Outerchr15:74892786..74896499hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383714
hg193714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660170
Supporting Variants
SamplesNA19430
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5756677
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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