A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524256



Internal ID15104863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24021660..24160925hg38UCSC Ensembl
InnerchrX:24039777..24179042hg19UCSC Ensembl
InnerchrX:23949698..24088963hg18UCSC Ensembl
InnerchrX:23799434..23938699hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38139266
hg19139266
hg18139266
hg17139266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700153
Samples
Known GenesEIF2S3, KLHL15, ZFX, ZFX-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524256
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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