A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035169



Internal ID18777700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112616002..112811301hg38UCSC Ensembl
Innerchr9:115378282..115573581hg19UCSC Ensembl
Innerchr9:114418103..114613402hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38195300
hg19195300
hg18195300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7701n100
Supporting Variantsnssv3695057
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035169
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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