A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495776



Internal ID20868970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87859201..87860100hg38UCSC Ensembl
chr15:88402432..88403331hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026982
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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