A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526383



Internal ID15453676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98448482..98582884hg38UCSC Ensembl
InnerchrX:97703480..97837882hg19UCSC Ensembl
InnerchrX:97590136..97724538hg18UCSC Ensembl
InnerchrX:97509625..97644027hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38134403
hg19134403
hg18134403
hg17134403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702680
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526383
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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