A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6942



Internal ID15190236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:41251549..41284127hg38UCSC Ensembl
Outerchr20:39880189..39912767hg19UCSC Ensembl
Outerchr20:39313603..39346181hg18UCSC Ensembl
Outerchr20:39313603..39346181hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3832579
hg1932579
hg1832579
hg1732579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3380
Supporting Variants
SamplesNA12156
Known GenesZHX3
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)nssv6942
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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