A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357471



Internal ID21015024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46420756..46510692hg38UCSC Ensembl
chr3:46462247..46552182hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3889937
hg1989936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100703
Samples
Known GenesLTF, RTP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357471
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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