A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11035



Internal ID15192987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:14771355..14968909hg38UCSC Ensembl
Outerchr20:14752001..14949555hg19UCSC Ensembl
Outerchr20:14700001..14897555hg18UCSC Ensembl
Outerchr20:14700001..14897555hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38197555
hg19197555
hg18197555
hg17197555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3300
Supporting Variants
SamplesNA15510
Known GenesMACROD2, MACROD2-AS1
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)nssv11035
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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