A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512183



Internal ID20885514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41537623..41541164hg38UCSC Ensembl
chr15:41829821..41833362hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383542
hg193542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023892
Samples
Known GenesRPAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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