A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527253



Internal ID15107860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70219663..70244558hg38UCSC Ensembl
InnerchrX:69439513..69464408hg19UCSC Ensembl
InnerchrX:69356238..69381133hg18UCSC Ensembl
InnerchrX:69222534..69247429hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3824896
hg1924896
hg1824896
hg1724896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703657
Samples
Known GenesAWAT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527253
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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