A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7705



Internal ID15536159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:15369675..15388400hg38UCSC Ensembl
Outerchr21:16741994..16760719hg19UCSC Ensembl
Outerchr21:15663865..15682590hg18UCSC Ensembl
Outerchr21:15663865..15682590hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3818726
hg1918726
hg1818726
hg1718726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3460
Supporting Variants
SamplesNA12156
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)nssv7705
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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