A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525162



Internal ID15452455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5669572..5684069hg38UCSC Ensembl
InnerchrX:5587613..5602110hg19UCSC Ensembl
InnerchrX:5597613..5612110hg18UCSC Ensembl
InnerchrX:5447349..5461846hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3814498
hg1914498
hg1814498
hg1714498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701236
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525162
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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