A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032113



Internal ID19121335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13861067..13923137hg38UCSC Ensembl
Innerchr9:13861066..13923136hg19UCSC Ensembl
Innerchr9:13851066..13913136hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3862071
hg1962071
hg1862071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7459n100
Supporting Variantsnssv3690616
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)nsv1032113
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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