A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560405



Internal ID16347814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119988665..119989653hg38UCSC Ensembl
Innerchr12:120426469..120427457hg19UCSC Ensembl
Innerchr12:118910852..118911840hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38989
hg19989
hg18989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803334
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560405
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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