A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507701



Internal ID20880995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44762026..44763879hg38UCSC Ensembl
chr15:45054224..45056077hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381854
hg191854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024577
Samples
Known GenesTRIM69
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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