A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515590



Internal ID15443201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8952896..9048808hg38UCSC Ensembl
InnerchrX:8920937..9016849hg19UCSC Ensembl
InnerchrX:8880937..8976849hg18UCSC Ensembl
InnerchrX:8730673..8826585hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3895913
hg1995913
hg1895913
hg1795913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667305, nssv679244, nssv664019, nssv691178, nssv683873, nssv664625, nssv678040, nssv667389, nssv667635, nssv669465, nssv669030, nssv689993, nssv656931, nssv655420
Samples
Known GenesFAM9B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515590
Frequency
Sample Size2026
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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