A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696337



Internal ID15432989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152069131..152104719hg38UCSC Ensembl
InnerchrX:151237603..151273191hg19UCSC Ensembl
InnerchrX:150988259..151023847hg18UCSC Ensembl
InnerchrX:150908171..150943759hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3835589
hg1935589
hg1835589
hg1735589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517791
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696337
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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