A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033659



Internal ID19122880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101320582..101492117hg38UCSC Ensembl
Innerchr7:100963863..101135398hg19UCSC Ensembl
Innerchr7:100750583..100922118hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38171536
hg19171536
hg18171536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3655304, nssv3755451
Samples
Known GenesCOL26A1, RABL5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033659
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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