A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021820



Internal ID19111038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97756411..97775189hg38UCSC Ensembl
Innerchr7:97385723..97404501hg19UCSC Ensembl
Innerchr7:97223659..97242437hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3818779
hg1918779
hg1818779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6535n100
Supporting Variantsnssv3655276
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021820
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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