A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376164



Internal ID21033717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69998601..69999400hg38UCSC Ensembl
chr4:70864318..70865117hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119056
Samples
Known GenesSTATH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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