A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559765



Internal ID16347174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:93092408..93111562hg38UCSC Ensembl
Innerchr12:93486184..93505338hg19UCSC Ensembl
Innerchr12:92010315..92029469hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3819155
hg1919155
hg1819155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800489
Samples
Known GenesLOC643339
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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