A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6961



Internal ID15190217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:46289083..46290060hg38UCSC Ensembl
Outerchr21:47708997..47709974hg19UCSC Ensembl
Outerchr21:46533425..46534402hg18UCSC Ensembl
Outerchr21:46533425..46534402hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg387184
hg197184
hg187184
hg177184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3547
Supporting Variants
SamplesNA12156
Known GenesYBEY
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)nssv6961
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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