A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017636



Internal ID19106853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19996294..20065115hg38UCSC Ensembl
Innerchr9:19996292..20065113hg19UCSC Ensembl
Innerchr9:19986292..20055113hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3868822
hg1968822
hg1868822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7471n100
Supporting Variantsnssv3690695
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)nsv1017636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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