A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507107



Internal ID20880395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43619801..43635900hg38UCSC Ensembl
chr15:43911999..43928098hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3816100
hg1916100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2511n223
Supporting Variantsnssv18186849
Samples
Known GenesCATSPER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507107
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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