A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3495252



Internal ID19082893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190892343..191053041hg38UCSC Ensembl
Innerchr1:190861473..191022171hg19UCSC Ensembl
Innerchr1:189128096..189288794hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38160699
hg19160699
hg18160699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013809
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3495252
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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