A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496157



Internal ID20869355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78501629..78504322hg38UCSC Ensembl
chr15:78793971..78796664hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382694
hg192694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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