A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7658



Internal ID15536206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:15675464..15720324hg38UCSC Ensembl
Outerchr20:15656109..15700969hg19UCSC Ensembl
Outerchr20:15604109..15648969hg18UCSC Ensembl
Outerchr20:15604109..15648969hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3844861
hg1944861
hg1844861
hg1744861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3303
Supporting Variants
SamplesNA12156
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)nssv7658
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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