A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748257



Internal ID15695527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:54487871..54526308hg38UCSC Ensembl
Innerchr10:56247631..56286068hg19UCSC Ensembl
Innerchr10:55917637..55956074hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3838438
hg1938438
hg1838438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550965
Supporting Variants
Samples
Known GenesPCDH15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748257
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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