A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511041



Internal ID20884365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84606887..84607701hg38UCSC Ensembl
chr15:85150118..85150932hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027225
Samples
Known GenesZSCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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