A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062700



Internal ID21971933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43947984..43947984hg38UCSC Ensembl
chr4:43950001..43950001hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062700
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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