A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516003



Internal ID15096610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:963886..968910hg38UCSC Ensembl
Innerchr12:1073052..1078076hg19UCSC Ensembl
Innerchr12:943313..948337hg18UCSC Ensembl
Innerchr12:943313..948337hg17UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg385025
hg195025
hg185025
hg175025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698086, nssv681116, nssv693566, nssv682484, nssv671144, nssv678091, nssv665662
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516003
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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