A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607014



Internal ID16394423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53392993..53539245hg38UCSC Ensembl
Innerchr7:53460686..53606938hg19UCSC Ensembl
Innerchr7:53428180..53574432hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38146253
hg19146253
hg18146253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11348n54
Supporting Variantsnssv1084643
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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