A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017782



Internal ID18760316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128288196..128306848hg38UCSC Ensembl
Innerchr7:127928249..127946901hg19UCSC Ensembl
Innerchr7:127715485..127734137hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3818653
hg1918653
hg1818653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6615n100
Supporting Variantsnssv3662182
Samples
Known GenesMGC27345
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017782
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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