A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001134



Internal ID20568174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42011089..42030896hg38UCSC Ensembl
chr12:42404891..42424698hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3819808
hg1919808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001134
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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