A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7667



Internal ID15536197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:24351022..24384158hg38UCSC Ensembl
Outerchr20:24331658..24364794hg19UCSC Ensembl
Outerchr20:24279658..24312794hg18UCSC Ensembl
Outerchr20:24279658..24312794hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg386256
hg196256
hg186256
hg176256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3339
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)nssv7667
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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