A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526672



Internal ID15453965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8856093..9048808hg38UCSC Ensembl
InnerchrX:8824134..9016849hg19UCSC Ensembl
InnerchrX:8784134..8976849hg18UCSC Ensembl
InnerchrX:8633870..8826585hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38192716
hg19192716
hg18192716
hg17192716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703004
Samples
Known GenesFAM9B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526672
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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