A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7674



Internal ID15536190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34278549..34323527hg38UCSC Ensembl
Outerchr20:32866355..32911333hg19UCSC Ensembl
Outerchr20:32330016..32374994hg18UCSC Ensembl
Outerchr20:32330016..32374994hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3844979
hg1944979
hg1844979
hg1744979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3358
Supporting Variants
SamplesNA12156
Known GenesAHCY
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)nssv7674
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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