A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7666



Internal ID15536198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:24255828..24289896hg38UCSC Ensembl
Outerchr20:24236464..24270532hg19UCSC Ensembl
Outerchr20:24184464..24218532hg18UCSC Ensembl
Outerchr20:24184464..24218532hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg385369
hg195369
hg185369
hg175369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3338
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)nssv7666
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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