A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522938



Internal ID15450231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5948582..5995721hg38UCSC Ensembl
InnerchrX:5866623..5913762hg19UCSC Ensembl
InnerchrX:5876623..5923762hg18UCSC Ensembl
InnerchrX:5726359..5773498hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3847140
hg1947140
hg1847140
hg1747140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698601
Samples
Known GenesNLGN4X
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522938
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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