A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370735



Internal ID21028288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123591050..123607983hg38UCSC Ensembl
chr3:123309897..123326830hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3816934
hg1916934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095242
Samples
Known GenesMYLK-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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