A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006113



Internal ID19095331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:95302946..95673447hg38UCSC Ensembl
Innerchr1:95768502..96139003hg19UCSC Ensembl
Innerchr1:95541090..95911591hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38370502
hg19370502
hg18370502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3466626
Samples
Known GenesFLJ31662
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006113
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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