A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525093



Internal ID15452386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:92378531..92383241hg38UCSC Ensembl
Innerchr12:92772307..92777017hg19UCSC Ensembl
Innerchr12:91296438..91301148hg18UCSC Ensembl
Innerchr12:91274775..91279485hg17UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg384711
hg194711
hg184711
hg174711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701152
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525093
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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