A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528179



Internal ID15108786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131166643..131546956hg38UCSC Ensembl
InnerchrX:130300617..130680930hg19UCSC Ensembl
InnerchrX:130128298..130508611hg18UCSC Ensembl
InnerchrX:130026152..130406465hg17UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38380314
hg19380314
hg18380314
hg17380314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704729
Samples
Known GenesIGSF1, OR13H1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528179
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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