A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517909



Internal ID15445202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151458320..151621244hg38UCSC Ensembl
InnerchrX:150626792..150789716hg19UCSC Ensembl
InnerchrX:150377450..150540372hg18UCSC Ensembl
InnerchrX:150297360..150460284hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38162925
hg19162925
hg18162923
hg17162925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695319
Samples
Known GenesPASD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517909
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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