A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099597



Internal ID15606097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152296623..152614320hg38UCSC Ensembl
Innerchr7:151993708..152311405hg19UCSC Ensembl
Innerchr7:151624641..151942338hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38317698
hg19317698
hg18317698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609048
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)nssv1099597
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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