A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019036



Internal ID18761569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128288388..128308069hg38UCSC Ensembl
Innerchr7:127928441..127948122hg19UCSC Ensembl
Innerchr7:127715677..127735358hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3819682
hg1919682
hg1819682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6615n100
Supporting Variantsnssv3662183
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)nsv1019036
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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