A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145038



Internal ID20712078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51292399..51292963hg38UCSC Ensembl
chr6:51157197..51157761hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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