A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515192



Internal ID20888551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44751114..44753981hg38UCSC Ensembl
chr17:42828482..42831349hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382868
hg192868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035867
Samples
Known GenesDBF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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