A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397488



Internal ID21055041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156935001..156940239hg38UCSC Ensembl
chr5:156362012..156367250hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg385239
hg195239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127719
Samples
Known GenesTIMD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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