A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607047



Internal ID16047770
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 StatusM
Merged Variantsdgv11354n54
Supporting Variantsnssv1084767
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)nsv607047
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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