A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370410



Internal ID21027963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75172320..75654345hg38UCSC Ensembl
chr3:75221471..75703496hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38482026
hg19482026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102319
Samples
Known GenesFAM86DP, MIR1324, MIR4444-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370410
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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