A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355707



Internal ID21013260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176717670..177455392hg38UCSC Ensembl
chr3:176435458..177173180hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38737723
hg19737723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211480
Samples
Known GenesLINC00501, LINC00578, TBL1XR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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