A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357800



Internal ID21015353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178288817..178289193hg38UCSC Ensembl
chr3:178006605..178006981hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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