A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073256



Internal ID21982489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26244172..26244172hg38UCSC Ensembl
chr4:26245794..26245794hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073256
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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