A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525937



Internal ID15453230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:153326898..153334291hg38UCSC Ensembl
Innerchr1:153299374..153306767hg19UCSC Ensembl
Innerchr1:151565998..151573391hg18UCSC Ensembl
Innerchr1:150112447..150119840hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg387394
hg197394
hg187394
hg177394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702143
Samples
Known GenesPGLYRP4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525937
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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