A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1616



Internal ID15545454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:13888138..13905135hg38UCSC Ensembl
Outerchr21:15260459..15277456hg19UCSC Ensembl
Outerchr21:14182330..14199327hg18UCSC Ensembl
Outerchr21:14182330..14199327hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3816998
hg1916998
hg1816998
hg1716998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3452
Supporting Variants
SamplesNA19240
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)nssv1616
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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