A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415219



Internal ID22473089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168383093..168383338hg38UCSC Ensembl
chr6:168783773..168784018hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415219
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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