A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6935



Internal ID15190243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:17868132..17897257hg38UCSC Ensembl
Outerchr20:17848776..17877901hg19UCSC Ensembl
Outerchr20:17796776..17825901hg18UCSC Ensembl
Outerchr20:17796776..17825901hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg387664
hg197664
hg187664
hg177664
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3312
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)nssv6935
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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