A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1691



Internal ID15194288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:142788232..142832624hg38UCSC Ensembl
Outerchr7:142494049..142530395hg19UCSC Ensembl
Outerchr7:142196044..142240517hg18UCSC Ensembl
Outerchr7:142002759..142047232hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3844393
hg1936347
hg1844474
hg1744474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5982
Supporting Variants
SamplesNA18555
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv1691
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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