A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016692



Internal ID19105909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7731398..7772496hg38UCSC Ensembl
Innerchr9:7731398..7772496hg19UCSC Ensembl
Innerchr9:7721398..7762496hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3841099
hg1941099
hg1841099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7393n100
Supporting Variantsnssv3758116, nssv3689109
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)nsv1016692
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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