A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10576



Internal ID15542222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:113770502..113783790hg38UCSC Ensembl
Outerchr7:113410557..113423845hg19UCSC Ensembl
Outerchr7:113197793..113211081hg18UCSC Ensembl
Outerchr7:113004508..113017796hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3813289
hg1913289
hg1813289
hg1713289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5911
Supporting Variants
SamplesNA18956
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)nssv10576
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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