A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375929



Internal ID21033482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158179601..158185800hg38UCSC Ensembl
chr4:159100753..159106952hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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