A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3582



Internal ID15201520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:26165303..26198965hg38UCSC Ensembl
Outerchr22:26561269..26594931hg19UCSC Ensembl
Outerchr22:24891269..24924931hg18UCSC Ensembl
Outerchr22:24885823..24919485hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg385624
hg195624
hg185624
hg175624
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5928
SamplesNA19129
Known GenesMIR1302-1, SEZ6L
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)nsv3582
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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