A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562407



Internal ID21886762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113353852..113354868hg38UCSC Ensembl
chr6:113675054..113676070hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562407
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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