A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520228



Internal ID15447521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:142795809..142864411hg38UCSC Ensembl
InnerchrX:141883595..141952197hg19UCSC Ensembl
InnerchrX:141711261..141779863hg18UCSC Ensembl
InnerchrX:141609115..141677717hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3868603
hg1968603
hg1868603
hg1768603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697294
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520228
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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