A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4524



Internal ID15192565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:15927189..15962052hg38UCSC Ensembl
Outerchr20:15907834..15942697hg19UCSC Ensembl
Outerchr20:15855834..15890697hg18UCSC Ensembl
Outerchr20:15855834..15890697hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg384874
hg194874
hg184874
hg174874
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3304
Supporting Variants
SamplesNA12878
Known GenesMACROD2
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)nssv4524
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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