A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524055



Internal ID15451348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:40811726..40902393hg38UCSC Ensembl
InnerchrX:40670979..40761646hg19UCSC Ensembl
InnerchrX:40555923..40646590hg18UCSC Ensembl
InnerchrX:40427233..40517900hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3890668
hg1990668
hg1890668
hg1790668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699921
Samples
Known GenesLOC100132831
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524055
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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