A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155235



Internal ID15877324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134703503..134718989hg38UCSC Ensembl
Innerchr7:134388255..134403741hg19UCSC Ensembl
Innerchr7:134038795..134054281hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3815487
hg1915487
hg1815487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608457
Supporting Variants
SamplesHGDP00968
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155235
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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