A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393657



Internal ID21051210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120080137..120080795hg38UCSC Ensembl
chr4:121001292..121001950hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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