A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500263



Internal ID20873488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38148284..38148756hg38UCSC Ensembl
chr15:38440485..38440957hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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