A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099479



Internal ID15952665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150348821..150418095hg38UCSC Ensembl
Innerchr7:150045910..150115183hg19UCSC Ensembl
Innerchr7:149676843..149746116hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3869275
hg1969274
hg1869274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608992
Supporting Variants
Samples
Known GenesLOC728743, 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)nssv1099479
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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