A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386041



Internal ID21043594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179219675..179293955hg38UCSC Ensembl
chr4:180140829..180215109hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3874281
hg1974281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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