A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525984



Internal ID15453277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:128049067..128050616hg38UCSC Ensembl
Innerchr12:128533612..128535161hg19UCSC Ensembl
Innerchr12:127099565..127101114hg18UCSC Ensembl
Innerchr12:127058492..127060041hg17UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg381550
hg191550
hg181550
hg171550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702203
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525984
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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