A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425476



Internal ID22483346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112006258..112008700hg38UCSC Ensembl
chr6:112327461..112329903hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382443
hg192443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425476
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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