A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326199



Internal ID20859333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161604876..161741092hg38UCSC Ensembl
chr1:161574666..161710882hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38136217
hg19136217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201278
Samples
Known GenesFCGR2B, FCGR3B, FCRLA, FCRLB, HSPA7, RPL31P11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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