A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382039



Internal ID21039592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174031565..174031966hg38UCSC Ensembl
chr4:174952716..174953117hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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