A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607015



Internal ID16394424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53399912..53522557hg38UCSC Ensembl
Innerchr7:53467605..53590250hg19UCSC Ensembl
Innerchr7:53435099..53557744hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38122646
hg19122646
hg18122646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11348n54
Supporting Variantsnssv1084644
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607015
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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