A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389716



Internal ID21047269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168129501..168131900hg38UCSC Ensembl
chr4:169050652..169053051hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115324
Samples
Known GenesANXA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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