A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364279



Internal ID21021832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141015345..141044164hg38UCSC Ensembl
chr3:140734187..140763006hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3828820
hg1928820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364279
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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