A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997739



Internal ID18810589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16886207..16949734hg38UCSC Ensembl
Innerchr1:17212702..17276229hg19UCSC Ensembl
Innerchr1:17085289..17148816hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3863528
hg1963528
hg1863528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv118n100
Supporting Variantsnssv3476961, nssv3469967
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)nsv997739
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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