A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389949



Internal ID21047502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119210082..119211835hg38UCSC Ensembl
chr4:120131237..120132990hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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