A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371691



Internal ID21029244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182740179..182810131hg38UCSC Ensembl
chr3:182457967..182527919hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3869953
hg1969953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211544
Samples
Known GenesATP11B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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