A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365027



Internal ID21022580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35215636..35217993hg38UCSC Ensembl
chr4:35217258..35219615hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382358
hg192358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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