A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518228



Internal ID15098835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:154601444..154719706hg38UCSC Ensembl
InnerchrX:153829693..153947981hg19UCSC Ensembl
InnerchrX:153482887..153601175hg18UCSC Ensembl
InnerchrX:153393397..153511685hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38118263
hg19118289
hg18118289
hg17118289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695657
Samples
Known GenesCTAG1A, CTAG1B, CTAG2, FAM223A, FAM223B, GAB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518228
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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