A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021131



Internal ID19110349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:162695..503337hg38UCSC Ensembl
Innerchr9:162695..503337hg19UCSC Ensembl
Innerchr9:152695..493337hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38340643
hg19340643
hg18340643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7346n100
Supporting Variantsnssv3690980
Samples
Known GenesC9orf66, CBWD1, DOCK8, KANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021131
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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