A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662



Internal ID15545204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98753303..98790970hg38UCSC Ensembl
Outerchr7:98382615..98388593hg19UCSC Ensembl
Outerchr7:98220551..98226529hg18UCSC Ensembl
Outerchr7:98027266..98033244hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3831321
hg1931321
hg1831321
hg1731321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5862
Supporting Variants
SamplesNA19240
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)nssv662
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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