A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361024



Internal ID21018577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14145142..14145686hg38UCSC Ensembl
chr3:14186642..14187186hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094304
Samples
Known GenesXPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361024
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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