A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515056



Internal ID20888413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86963005..86963607hg38UCSC Ensembl
chr15:87506236..87506838hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027863
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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