A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368820



Internal ID21026373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104198674..104199161hg38UCSC Ensembl
chr3:103917518..103918005hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092336
Samples
Known GenesMIR548A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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