A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154835



Internal ID22085340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:50785433..50792569hg38UCSC Ensembl
Outerchr12:50779628..50795147hg38UCSC Ensembl
Innerchr12:51179216..51186352hg19UCSC Ensembl
Outerchr12:51173411..51188930hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3815520
hg1915520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009238
Samples
Known GenesATF1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154835
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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