A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505231



Internal ID20878498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97958501..97963900hg38UCSC Ensembl
chr15:98501731..98507130hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180351
Samples
Known GenesARRDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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