A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1599



Internal ID15198787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34978502..35010725hg38UCSC Ensembl
Outerchr20:33566305..33598528hg19UCSC Ensembl
Outerchr20:33029966..33062189hg18UCSC Ensembl
Outerchr20:33029966..33062189hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg388770
hg198770
hg188770
hg178770
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3362
Supporting Variants
SamplesNA19240
Known GenesMIR499A, MIR499B, MYH7B, TRPC4AP
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)nssv1599
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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