A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7701



Internal ID15536163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:61306732..61340386hg38UCSC Ensembl
Outerchr20:59881788..59915442hg19UCSC Ensembl
Outerchr20:59315183..59348837hg18UCSC Ensembl
Outerchr20:59315183..59348837hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385786
hg195786
hg185786
hg175786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3437
Supporting Variants
SamplesNA12156
Known GenesCDH4
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)nssv7701
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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