A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9601



Internal ID15539713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:13845848..13900409hg38UCSC Ensembl
Outerchr21:15218169..15272730hg19UCSC Ensembl
Outerchr21:14140040..14194601hg18UCSC Ensembl
Outerchr21:14140040..14194601hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3854562
hg1954562
hg1854562
hg1754562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3452
Supporting Variants
SamplesNA18507
Known GenesC21orf15
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)nssv9601
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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