A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499899



Internal ID20873124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92718174..92733167hg38UCSC Ensembl
chr15:93261404..93276397hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3814994
hg1914994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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