A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6983



Internal ID15190195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36727685..36767080hg38UCSC Ensembl
Outerchr22:37123730..37163124hg19UCSC Ensembl
Outerchr22:35453676..35493070hg18UCSC Ensembl
Outerchr22:35448230..35487624hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3839396
hg1939395
hg1839395
hg1739395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3617
Supporting Variants
SamplesNA12156
Known GenesIFT27
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)nssv6983
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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