A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527262



Internal ID15107869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56731798..56748393hg38UCSC Ensembl
InnerchrX:56758231..56774826hg19UCSC Ensembl
InnerchrX:56774956..56791551hg18UCSC Ensembl
InnerchrX:56641252..56657847hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3816596
hg1916596
hg1816596
hg1716596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703668
Samples
Known GenesLOC550643, UQCRBP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527262
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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