A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017021



Internal ID19106238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7731398..7764735hg38UCSC Ensembl
Innerchr9:7731398..7764735hg19UCSC Ensembl
Innerchr9:7721398..7754735hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3833338
hg1933338
hg1833338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7393n100
Supporting Variantsnssv3689108
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)nsv1017021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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