A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661604



Internal ID9927709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42350296..42350779hg38UCSC Ensembl
Outerchr15:42350259..42350829hg38UCSC Ensembl
Innerchr15:42642494..42642977hg19UCSC Ensembl
Outerchr15:42642457..42643027hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5594853, essv6158965, essv6291892, essv6324736, essv5482310
SamplesNA19355, NA19381, NA20282, NA19430, NA19463
Known GenesGANC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661604
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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