A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516826



Internal ID15444119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116807112..116908132hg38UCSC Ensembl
InnerchrX:115941080..116042100hg19UCSC Ensembl
InnerchrX:115825108..115926128hg18UCSC Ensembl
InnerchrX:115722962..115823982hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38101021
hg19101021
hg18101021
hg17101021
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656627, nssv689137, nssv700362, nssv682666, nssv687423, nssv654274, nssv697293, nssv684918, nssv677350
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516826
Frequency
Sample Size2026
Observed Gain5
Observed Loss4
Observed Complex0
Frequencyn/a


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