A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033783



Internal ID18776316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71490292..71558892hg38UCSC Ensembl
Innerchr7:70955277..71023877hg19UCSC Ensembl
Innerchr7:70593213..70661813hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3868601
hg1968601
hg1868601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755310
Samples
Known GenesWBSCR17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033783
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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