A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7475



Internal ID15189703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:26631164..26673011hg38UCSC Ensembl
Outerchr2:26854032..26895879hg19UCSC Ensembl
Outerchr2:26707536..26749383hg18UCSC Ensembl
Outerchr2:26765683..26807530hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3841848
hg1941848
hg1841848
hg1741848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2651
Supporting Variants
SamplesNA12156
Known GenesCIB4
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)nssv7475
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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