A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519945



Internal ID15447238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:147303051..147349540hg38UCSC Ensembl
InnerchrX:146384569..146431058hg19UCSC Ensembl
InnerchrX:146192261..146238750hg18UCSC Ensembl
InnerchrX:146090115..146136604hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3846490
hg1946490
hg1846490
hg1746490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697140
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519945
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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