A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2323



Internal ID15540819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1576966..1615498hg38UCSC Ensembl
Outerchr20:1557612..1596144hg19UCSC Ensembl
Outerchr20:1505612..1544144hg18UCSC Ensembl
Outerchr20:1505612..1544144hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838533
hg1938533
hg1838533
hg1738533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3253
Supporting Variants
SamplesNA18555
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)nssv2323
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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