A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073637



Internal ID21982870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181444864..181444864hg38UCSC Ensembl
chr5:180871865..180871865hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073637
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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