A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385864



Internal ID21043417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35873501..35879200hg38UCSC Ensembl
chr5:35873603..35879302hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129805
Samples
Known GenesIL7R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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