A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323219



Internal ID20856336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161511475..161593135hg38UCSC Ensembl
chr1:161481265..161562925hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881661
hg1981661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv402n223
Supporting Variantsnssv18053258
Samples
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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