A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444775



Internal ID22502645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75306792..75306841hg38UCSC Ensembl
chr6:76016508..76016557hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444775
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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