A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495699



Internal ID20868893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90846087..90846586hg38UCSC Ensembl
chr15:91389317..91389816hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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