A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525381



Internal ID15452674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121954738..122016686hg38UCSC Ensembl
InnerchrX:121088591..121150539hg19UCSC Ensembl
InnerchrX:120916272..120978220hg18UCSC Ensembl
InnerchrX:120814126..120876074hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3861949
hg1961949
hg1861949
hg1761949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701503
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525381
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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