A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513859



Internal ID20887208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94929989..94943826hg38UCSC Ensembl
chr15:95473218..95487055hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3813838
hg1913838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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