A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514983



Internal ID20888338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31155121..31158986hg38UCSC Ensembl
chr15:31447324..31451189hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383866
hg193866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023507
Samples
Known GenesTRPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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