A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026994



Internal ID19116213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41475094..41892854hg19UCSC Ensembl
Innerchr9:41465094..41882854hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg19417761
hg18417761
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7541n100
Supporting Variantsnssv3690147, nssv3690145, nssv3690144, nssv3690146, nssv3690143
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)nsv1026994
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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