A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145901



Internal ID20712941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56145201..56146400hg38UCSC Ensembl
chr6:56009999..56011198hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399925
Supporting Variants
Samples
Known GenesCOL21A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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