A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501593



Internal ID20874829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95893113..95899582hg38UCSC Ensembl
chr15:96436342..96442811hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg386470
hg196470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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