A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063679



Internal ID21972912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157121625..157121625hg38UCSC Ensembl
chr3:156839414..156839414hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543278
Samples
Known GenesLINC00880
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063679
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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