A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522544



Internal ID15449837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:137477740..137690759hg38UCSC Ensembl
InnerchrX:136559899..136772918hg19UCSC Ensembl
InnerchrX:136387565..136600584hg18UCSC Ensembl
InnerchrX:136285419..136498438hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38213020
hg19213020
hg18213020
hg17213020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705924
Samples
Known GenesZIC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522544
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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