A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607050



Internal ID16047773
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 StatusM
Merged Variantsdgv11354n54
Supporting Variantsnssv1084769
Samples
Known GenesMIR3147, ZNF716
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607050
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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