A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522678



Internal ID15449971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:39429817..39433445hg38UCSC Ensembl
InnerchrX:39289071..39292699hg19UCSC Ensembl
InnerchrX:39174015..39177643hg18UCSC Ensembl
InnerchrX:39045286..39048914hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg383629
hg193629
hg183629
hg173629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706086
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522678
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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