A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526183



Internal ID15453476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:32378278..32382881hg38UCSC Ensembl
Innerchr12:32531212..32535815hg19UCSC Ensembl
Innerchr12:32422479..32427082hg18UCSC Ensembl
Innerchr12:32422479..32427082hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg384604
hg194604
hg184604
hg174604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702445
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526183
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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