A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033447



Internal ID19122669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149493936..149622348hg38UCSC Ensembl
Innerchr7:149191027..149319439hg19UCSC Ensembl
Innerchr7:148821960..148950372hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38128413
hg19128413
hg18128413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674237
Samples
Known GenesZNF746, ZNF767
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033447
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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