A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9872



Internal ID15193261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42115497..42127710hg38UCSC Ensembl
Outerchr22:42511501..42523712hg19UCSC Ensembl
Outerchr22:40841447..40853656hg18UCSC Ensembl
Outerchr22:40836001..40848210hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3811582
hg1911582
hg1811582
hg1711582
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3642
Supporting Variants
SamplesNA18507
Known GenesCYP2D6, NDUFA6-AS1
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)nssv9872
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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