A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504189



Internal ID20877450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73702247..73703688hg38UCSC Ensembl
chr15:73994588..73996029hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026649
Samples
Known GenesCD276
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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