A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997424



Internal ID19156960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163273064..163449138hg38UCSC Ensembl
Innerchr3:162990852..163166926hg19UCSC Ensembl
Innerchr3:164473546..164649620hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38176075
hg19176075
hg18176075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738246, nssv3738245
Samples
Known GenesCT64
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997424
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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