A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7657



Internal ID15189521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:14891468..14918195hg38UCSC Ensembl
Outerchr20:14872114..14898841hg19UCSC Ensembl
Outerchr20:14820114..14846841hg18UCSC Ensembl
Outerchr20:14820114..14846841hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3826728
hg1926728
hg1826728
hg1726728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3300
Supporting Variants
SamplesNA12156
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)nssv7657
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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