A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389300



Internal ID21046853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145113698..145114332hg38UCSC Ensembl
chr4:146034850..146035484hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108859
Samples
Known GenesABCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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