A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515400



Internal ID20888759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36626053..36629076hg38UCSC Ensembl
chr15:36918254..36921277hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383024
hg193024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024352
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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