A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374934



Internal ID21032487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169350701..169351600hg38UCSC Ensembl
chr3:169068489..169069388hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097467
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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