A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575190



Internal ID21767233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69999534..70010861hg38UCSC Ensembl
chr6:70709426..70720753hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811328
hg1911328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003509
Supporting Variants
Samples
Known GenesCOL19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575190
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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