A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032474



Internal ID19121696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2773573..2804799hg38UCSC Ensembl
Innerchr9:2773573..2804799hg19UCSC Ensembl
Innerchr9:2763573..2794799hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3831227
hg1931227
hg1831227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758085
Samples
Known GenesKIAA0020
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032474
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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