A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7603



Internal ID15536261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:206850925..206896246hg38UCSC Ensembl
Outerchr2:207715649..207760970hg19UCSC Ensembl
Outerchr2:207423894..207469215hg18UCSC Ensembl
Outerchr2:207541155..207586476hg17UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3845322
hg1945322
hg1845322
hg1745322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3127
Supporting Variants
SamplesNA12156
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)nssv7603
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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