A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505299



Internal ID20878567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81257632..81265726hg38UCSC Ensembl
chr15:81549973..81558067hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg388095
hg198095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026455
Samples
Known GenesIL16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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