A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032897



Internal ID19122119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155691696..155739205hg38UCSC Ensembl
Innerchr7:155484390..155531899hg19UCSC Ensembl
Innerchr7:155177151..155224660hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3847510
hg1947510
hg1847510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6767n100
Supporting Variantsnssv3674700
Samples
Known GenesRBM33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032897
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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