A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099602



Internal ID15606102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152336108..152481870hg38UCSC Ensembl
Innerchr7:152033193..152178955hg19UCSC Ensembl
Innerchr7:151664126..151809888hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38145763
hg19145763
hg18145763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609054
Supporting Variants
Samples
Known GenesFABP5P3, KMT2C, LINC01003
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099602
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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