A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526743



Internal ID15107350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30298063..30441396hg38UCSC Ensembl
InnerchrX:30316180..30459513hg19UCSC Ensembl
InnerchrX:30226101..30369434hg18UCSC Ensembl
InnerchrX:30075837..30219170hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38143334
hg19143334
hg18143334
hg17143334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv505n21
Supporting Variantsnssv703086
Samples
Known GenesNR0B1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526743
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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