A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369658



Internal ID21027211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46433915..46659106hg38UCSC Ensembl
chr3:46475406..46700596hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38225192
hg19225191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209281
Samples
Known GenesLOC100132146, LRRC2, LRRC2-AS1, LTF, RTP3, TDGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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