A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413689



Internal ID22471559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124890318..124905179hg38UCSC Ensembl
chr6:125211464..125226325hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3814862
hg1914862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413689
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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