A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507635



Internal ID20880929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44758026..44758488hg38UCSC Ensembl
chr15:45050224..45050686hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024576
Samples
Known GenesTRIM69
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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