A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513432



Internal ID20886776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66670496..66673675hg38UCSC Ensembl
chr15:66962834..66966013hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383180
hg193180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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