A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676



Internal ID15545278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:109788790..109827154hg38UCSC Ensembl
Outerchr7:109428847..109467211hg19UCSC Ensembl
Outerchr7:109216083..109254447hg18UCSC Ensembl
Outerchr7:109022798..109061162hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3838365
hg1938365
hg1838365
hg1738365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896
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)nssv676
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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