A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412814



Internal ID22470684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107138510..107139938hg38UCSC Ensembl
chr6:107459714..107461142hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381429
hg191429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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