A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528977



Internal ID15456270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25880353..25881720hg38UCSC Ensembl
Innerchr12:26033286..26034653hg19UCSC Ensembl
Innerchr12:25924553..25925920hg18UCSC Ensembl
Innerchr12:25924553..25925920hg17UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381368
hg191368
hg181368
hg171368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705676
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528977
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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