A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779666



Internal ID19160827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61744448..61825972hg38UCSC Ensembl
Innerchr6:62454353..62535877hg19UCSC Ensembl
Innerchr6:62512312..62593836hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3881525
hg1981525
hg1881525
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890858
Supporting Variants
Samples
Known GenesKHDRBS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779666
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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