A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029718



Internal ID19118937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85785638..85874294hg38UCSC Ensembl
Innerchr7:85414954..85503610hg19UCSC Ensembl
Innerchr7:85252890..85341546hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3888657
hg1988657
hg1888657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6521n100
Supporting Variantsnssv3755428
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)nsv1029718
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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