A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412173



Internal ID22470043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103015145..103218776hg38UCSC Ensembl
chr6:103463020..103666651hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38203632
hg19203632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412173
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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