A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411682



Internal ID21069235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157179499..157180135hg38UCSC Ensembl
chr5:156606510..156607146hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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