A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2537



Internal ID15540584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:109242245..109267995hg38UCSC Ensembl
Outerchr5:108577946..108603696hg19UCSC Ensembl
Outerchr5:108605845..108631595hg18UCSC Ensembl
Outerchr5:108605845..108631595hg17UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3825751
hg1925751
hg1825751
hg1725751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4955
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)nssv2537
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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