A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527395



Internal ID15454688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138386305..138404006hg38UCSC Ensembl
InnerchrX:137468464..137486165hg19UCSC Ensembl
InnerchrX:137296130..137313831hg18UCSC Ensembl
InnerchrX:137193984..137211685hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3817702
hg1917702
hg1817702
hg1717702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703830
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527395
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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