A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033423



Internal ID19122645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6814467..6893147hg38UCSC Ensembl
Innerchr7:6854098..6932778hg19UCSC Ensembl
Innerchr7:6820623..6899303hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3878681
hg1978681
hg1878681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6244n100
Supporting Variantsnssv3655076
Samples
Known GenesCCZ1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033423
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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