A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334058



Internal ID20867239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161514001..161595700hg38UCSC Ensembl
chr1:161483791..161565490hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881700
hg1981700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv401n223
Supporting Variantsnssv18201010
Samples
Known GenesFCGR2A, FCGR2C, FCGR3A, HSPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334058
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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