A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006248



Internal ID20573289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93930832..93931714hg38UCSC Ensembl
chr12:94324608..94325490hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006248
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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