A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498477



Internal ID20871688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31097177..31109679hg38UCSC Ensembl
chr15:31389380..31401882hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3812503
hg1912503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023504
Samples
Known GenesTRPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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