A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033114



Internal ID19122336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79688502..79779397hg38UCSC Ensembl
Innerchr7:79317818..79408713hg19UCSC Ensembl
Innerchr7:79155754..79246649hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3890896
hg1990896
hg1890896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6512n100
Supporting Variantsnssv3657182
Samples
Known GenesMIR548M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033114
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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