A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030948



Internal ID18773480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33140791..33274464hg38UCSC Ensembl
Innerchr9:33140789..33274462hg19UCSC Ensembl
Innerchr9:33130789..33264462hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38133674
hg19133674
hg18133674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7516n100
Supporting Variantsnssv3688871
Samples
Known GenesB4GALT1, BAG1, CHMP5, LOC101929639, SPINK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030948
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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