A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519898



Internal ID15447191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140804585..140804926hg38UCSC Ensembl
InnerchrX:139886750..139887091hg19UCSC Ensembl
InnerchrX:139714416..139714757hg18UCSC Ensembl
InnerchrX:139612270..139612611hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38342
hg19342
hg18342
hg17342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672294, nssv677369, nssv659377, nssv691549
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519898
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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