A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526288



Internal ID15106895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:96486039..96506039hg38UCSC Ensembl
Innerchr12:96879817..96899817hg19UCSC Ensembl
Innerchr12:95403948..95423948hg18UCSC Ensembl
Innerchr12:95382285..95402285hg17UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3820001
hg1920001
hg1820001
hg1720001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702568
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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