A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6922



Internal ID15536941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1579413..1616101hg38UCSC Ensembl
Outerchr20:1560059..1596747hg19UCSC Ensembl
Outerchr20:1508059..1544747hg18UCSC Ensembl
Outerchr20:1508059..1544747hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836689
hg1936689
hg1836689
hg1736689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3253
Supporting Variants
SamplesNA12156
Known GenesSIRPB1
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)nssv6922
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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