A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558240



Internal ID21882595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71329041..71329041hg38UCSC Ensembl
chr6:72038744..72038744hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385932
hg195932
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558240
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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