A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9664



Internal ID15193453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:55082169..55126059hg38UCSC Ensembl
Outerchr5:54377997..54421887hg19UCSC Ensembl
Outerchr5:54413754..54457644hg18UCSC Ensembl
Outerchr5:54413754..54457644hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3843891
hg1943891
hg1843891
hg1743891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4833
Supporting Variants
SamplesNA18507
Known GenesCDC20B, GZMA
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)nssv9664
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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