A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504482



Internal ID20877743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71183101..71185600hg38UCSC Ensembl
chr15:71475440..71477939hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2577n223
Supporting Variantsnssv18026379
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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