A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525660



Internal ID15106267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:134579742..134604314hg38UCSC Ensembl
InnerchrX:133713772..133738344hg19UCSC Ensembl
InnerchrX:133541438..133566010hg18UCSC Ensembl
InnerchrX:133439292..133463864hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3824573
hg1924573
hg1824573
hg1724573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701816
Samples
Known GenesPLAC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525660
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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