A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7721



Internal ID15536143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:36867222..36900927hg38UCSC Ensembl
Outerchr21:38239522..38273227hg19UCSC Ensembl
Outerchr21:37161392..37195097hg18UCSC Ensembl
Outerchr21:37161392..37195097hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg385734
hg195734
hg185734
hg175734
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3508
Supporting Variants
SamplesNA12156
Known GenesHLCS
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)nssv7721
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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