A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084767



Internal ID15591267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57118123..57549195hg38UCSC Ensembl
Innerchr7:57185830..57608901hg19UCSC Ensembl
Innerchr7:57189772..57612843hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38431073
hg19423072
hg18423072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607047
Supporting Variants
Samples
Known GenesGUSBP10, MIR3147, ZNF479, ZNF716
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1084767
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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