A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519551



Internal ID15100158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37491775..37509678hg38UCSC Ensembl
Innerchr1:37957376..37975279hg19UCSC Ensembl
Innerchr1:37729963..37747866hg18UCSC Ensembl
Innerchr1:37626469..37644372hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3817904
hg1917904
hg1817904
hg1717904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656832, nssv684557
Samples
Known GenesMEAF6, MIR5581
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519551
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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