A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527422



Internal ID15454715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76045863..76154105hg38UCSC Ensembl
InnerchrX:75265698..75373940hg19UCSC Ensembl
InnerchrX:75182077..75290344hg18UCSC Ensembl
InnerchrX:75048373..75156640hg17UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38108243
hg19108243
hg18108268
hg17108268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703860
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527422
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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