A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528014



Internal ID15108621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135359359..135467699hg38UCSC Ensembl
InnerchrX:134493284..134601624hg19UCSC Ensembl
InnerchrX:134320950..134429290hg18UCSC Ensembl
InnerchrX:134218804..134327144hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38108341
hg19108341
hg18108341
hg17108341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704542
Samples
Known GenesLINC00086, LOC100506790, ZNF449
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528014
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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