A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413838



Internal ID21071391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95531610..95535624hg38UCSC Ensembl
chr5:94867314..94871328hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg384015
hg194015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135604
Samples
Known GenesTTC37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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