A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608991



Internal ID16396400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150338437..150407322hg38UCSC Ensembl
Innerchr7:150035526..150104410hg19UCSC Ensembl
Innerchr7:149666459..149735343hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3868886
hg1968885
hg1868885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11718n54
Supporting Variantsnssv1099478
Samples
Known GenesLOC728743, RARRES2, REPIN1, RNU6-33P, RNU6-34P, ZNF775
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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