A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524834



Internal ID15105441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37496012..37585984hg38UCSC Ensembl
Innerchr1:37961613..38051585hg19UCSC Ensembl
Innerchr1:37734200..37824172hg18UCSC Ensembl
Innerchr1:37630706..37720678hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3889973
hg1989973
hg1889973
hg1789973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700835
Samples
Known GenesDNALI1, GNL2, MEAF6, MIR5581, SNIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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