A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375164



Internal ID21032717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137416001..137541000hg38UCSC Ensembl
chr3:137134843..137259842hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38125000
hg19125000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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