A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522756



Internal ID15450049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:149341577..149442139hg38UCSC Ensembl
InnerchrX:148423107..148523670hg19UCSC Ensembl
InnerchrX:148230829..148331596hg18UCSC Ensembl
InnerchrX:148128683..148229450hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38100563
hg19100564
hg18100768
hg17100768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698395
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522756
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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