A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505281



Internal ID20878548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51550101..51551600hg38UCSC Ensembl
chr15:51842298..51843797hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024026
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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