A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608161



Internal ID16395570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111264170..111546637hg38UCSC Ensembl
Innerchr7:110904226..111186693hg19UCSC Ensembl
Innerchr7:110691462..110973929hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38282468
hg19282468
hg18282468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11572n54
Supporting Variantsnssv1155374
Samples1780854097_A
Known GenesIMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608161
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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