A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6984



Internal ID15536880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:37012269..37043670hg38UCSC Ensembl
Outerchr22:37408310..37439710hg19UCSC Ensembl
Outerchr22:35738256..35769656hg18UCSC Ensembl
Outerchr22:35732810..35764210hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg388036
hg198036
hg188036
hg178036
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3622
Supporting Variants
SamplesNA12156
Known GenesMPST, TST
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)nssv6984
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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