A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561840



Internal ID21886195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113364873..113364873hg38UCSC Ensembl
chr6:113686075..113686075hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561840
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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