A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084769



Internal ID15937955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57186940..57530097hg38UCSC Ensembl
Innerchr7:57254647..57589803hg19UCSC Ensembl
Innerchr7:57258589..57593745hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38343158
hg19335157
hg18335157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607050
Supporting Variants
Samples
Known GenesMIR3147, ZNF716
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1084769
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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