A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390875



Internal ID21048428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:172702901..172705100hg38UCSC Ensembl
chr4:173624052..173626251hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112319
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390875
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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