A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497456



Internal ID20870662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65523701..65528800hg38UCSC Ensembl
chr15:65816039..65821138hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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