A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358190



Internal ID21015743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176364944..176406914hg38UCSC Ensembl
chr3:176082732..176124702hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3841971
hg1941971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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