A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6071802



Internal ID8963010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82371170..82482204hg38UCSC Ensembl
Outerchr15:82370798..82482570hg38UCSC Ensembl
Innerchr15:83039916..83150922hg19UCSC Ensembl
Outerchr15:83039545..83151292hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38111773
hg19111748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666932
Supporting Variants
SamplesHG00533
Known GenesCSPG4P8, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, UBE2Q2P2, UBE2Q2P3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6071802
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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