A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516386



Internal ID15443679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146648726..147040618hg38UCSC Ensembl
Innerchr3:146366513..146758405hg19UCSC Ensembl
Innerchr3:147849203..148241095hg18UCSC Ensembl
Innerchr3:147849211..148241103hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38391893
hg19391893
hg18391893
hg17391893
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703778, nssv667949, nssv701203, nssv691231
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516386
Frequency
Sample Size2026
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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