A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1682



Internal ID15540965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:113774697..113783141hg38UCSC Ensembl
Outerchr7:113414752..113423196hg19UCSC Ensembl
Outerchr7:113201988..113210432hg18UCSC Ensembl
Outerchr7:113008703..113017147hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg388445
hg198445
hg188445
hg178445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911
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)nssv1682
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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