A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503413



Internal ID20876668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75611472..75623321hg38UCSC Ensembl
chr15:75903813..75915662hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3811850
hg1911850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025731
Samples
Known GenesSNUPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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