A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608159



Internal ID16395568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111211497..111529171hg38UCSC Ensembl
Innerchr7:110851553..111169227hg19UCSC Ensembl
Innerchr7:110638789..110956463hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38317675
hg19317675
hg18317675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11572n54
Supporting Variantsnssv1092690
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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