A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008279



Internal ID19097498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16912960..16934111hg38UCSC Ensembl
Innerchr1:17239455..17260606hg19UCSC Ensembl
Innerchr1:17112042..17133193hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821152
hg1921152
hg1821152
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv124n100
Supporting Variantsnssv3467090, nssv3700277, nssv3700276
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008279
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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