A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018682



Internal ID19107899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41475094..41854479hg19UCSC Ensembl
Innerchr9:41465094..41844479hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg19379386
hg18379386
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7541n100
Supporting Variantsnssv3690140, nssv3690142, nssv3690141
Samples
Known GenesLOC653501, SPATA31A5, SPATA31A7, ZNF658B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018682
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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