A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559852



Internal ID16347261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:97919457..97949056hg38UCSC Ensembl
Innerchr12:98313235..98342834hg19UCSC Ensembl
Innerchr12:96837366..96866965hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3829600
hg1929600
hg1829600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800873
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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