A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500085



Internal ID20873310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69071246..69071544hg38UCSC Ensembl
chr15:69363586..69363884hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026289
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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