A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033095



Internal ID18775629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149810995..150084783hg38UCSC Ensembl
Innerchr7:149508083..149781872hg19UCSC Ensembl
Innerchr7:149139016..149412805hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38273789
hg19273790
hg18273790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757721
Samples
Known GenesATP6V0E2, ATP6V0E2-AS1, SSPO, ZNF862
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033095
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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