A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361607



Internal ID21019160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58624424..58624768hg38UCSC Ensembl
chr3:58610151..58610495hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102950
Samples
Known GenesFAM107A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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