A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692426



Internal ID18990707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5915640..6114652hg38UCSC Ensembl
Innerchr9:5915640..6114652hg19UCSC Ensembl
Innerchr9:5905640..6104652hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38199013
hg19199013
hg18199013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015450
Supporting Variants
Samples
Known GenesKIAA2026, MIR4665, RANBP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692426
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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