A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034122



Internal ID19123344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38503816..38568172hg38UCSC Ensembl
Innerchr9:38503813..38568169hg19UCSC Ensembl
Innerchr9:38493813..38558169hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3864357
hg1964357
hg1864357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755936
Samples
Known GenesFAM95C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034122
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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