A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055499



Internal ID21964732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14174322..14174322hg38UCSC Ensembl
chr3:14215822..14215822hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545712
Samples
Known GenesXPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055499
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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