A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6982



Internal ID15190196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35721621..35736472hg38UCSC Ensembl
Outerchr22:36117668..36132519hg19UCSC Ensembl
Outerchr22:34447614..34462465hg18UCSC Ensembl
Outerchr22:34442168..34457019hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg387394
hg197394
hg187394
hg177394
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3612
Supporting Variants
SamplesNA12156
Known GenesAPOL5
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)nssv6982
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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