A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388961



Internal ID21046514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38690684..38691287hg38UCSC Ensembl
chr4:38692305..38692908hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116025
Samples
Known GenesKLF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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