A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009012



Internal ID22070643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30084564..30091000hg38UCSC Ensembl
Outerchr12:30082648..30091017hg38UCSC Ensembl
Innerchr12:30237497..30243933hg19UCSC Ensembl
Outerchr12:30235581..30243950hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg388370
hg198370
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154821
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009012
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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