A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075993



Internal ID21985226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187304419..187304419hg38UCSC Ensembl
chr4:188225573..188225573hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554157
Samples
Known GenesLOC339975
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075993
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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