A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423011



Internal ID22480881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113520888..113521050hg38UCSC Ensembl
chr6:113842090..113842252hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423011
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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