A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362168



Internal ID21019721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99947563..99984147hg38UCSC Ensembl
chr3:99666407..99702991hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3836585
hg1936585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105070
Samples
Known GenesCMSS1, FILIP1L, MIR3921, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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