A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524776



Internal ID15105383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:80647670..80757308hg38UCSC Ensembl
InnerchrX:79903169..80012807hg19UCSC Ensembl
InnerchrX:79789825..79899463hg18UCSC Ensembl
InnerchrX:79709314..79818952hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38109639
hg19109639
hg18109639
hg17109639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700767
Samples
Known GenesBRWD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524776
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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