A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496205



Internal ID20869404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87488046..87503226hg38UCSC Ensembl
chr15:88031277..88046457hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3815181
hg1915181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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