A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5793



Internal ID15203952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74400259..74443070hg38UCSC Ensembl
Outerchr7:73814589..73857400hg19UCSC Ensembl
Outerchr7:73452525..73495336hg18UCSC Ensembl
Outerchr7:73259240..73302051hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3842812
hg1942812
hg1842812
hg1742812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2666
SamplesNA18555
Known GenesCLIP2
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)nsv5793
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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