A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9563



Internal ID15539751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:6552992..6605919hg38UCSC Ensembl
Outerchr2:6693124..6746051hg19UCSC Ensembl
Outerchr2:6610575..6663502hg18UCSC Ensembl
Outerchr2:6643722..6696649hg17UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3852928
hg1952928
hg1852928
hg1752928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2595
Supporting Variants
SamplesNA18507
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)nssv9563
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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