A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513841



Internal ID20887190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87585577..87680510hg38UCSC Ensembl
chr15:88128808..88223741hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3894934
hg1994934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2622n223
Supporting Variantsnssv18182245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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