A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv505n21



Internal ID20132226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30298063..30441396hg38UCSC Ensembl
chrX:30316180..30459513hg19UCSC Ensembl
chrX:30226101..30369434hg18UCSC Ensembl
chrX: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 Variants
Supporting Variantsnsv520655, nsv526743
Samples
Known GenesNR0B1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv505n21
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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