A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384132



Internal ID21041685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141529372..141529785hg38UCSC Ensembl
chr4:142450525..142450938hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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