A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033642



Internal ID19122863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89699437..89927701hg38UCSC Ensembl
Innerchr7:89328751..89557015hg19UCSC Ensembl
Innerchr7:89166687..89394951hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38228265
hg19228265
hg18228265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6528n100
Supporting Variantsnssv3655218
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)nsv1033642
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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