A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525958



Internal ID15453251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:91914451..91918651hg38UCSC Ensembl
Innerchr12:92308227..92312427hg19UCSC Ensembl
Innerchr12:90832358..90836558hg18UCSC Ensembl
Innerchr12:90810695..90814895hg17UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg384201
hg194201
hg184201
hg174201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702168
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525958
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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