A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2263



Internal ID15541687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:61631589..61676074hg38UCSC Ensembl
Outerchr2:61858724..61903209hg19UCSC Ensembl
Outerchr2:61712228..61756713hg18UCSC Ensembl
Outerchr2:61770375..61814860hg17UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3844486
hg1944486
hg1844486
hg1744486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2750
Supporting Variants
SamplesNA18555
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)nssv2263
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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