A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700269



Internal ID15436921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:22494959..22518578hg38UCSC Ensembl
InnerchrX:22513076..22536695hg19UCSC Ensembl
InnerchrX:22422997..22446616hg18UCSC Ensembl
InnerchrX:22272733..22296352hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3823620
hg1923620
hg1823620
hg1723620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524358
Supporting Variants
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700269
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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