A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500145



Internal ID20873370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100877701..100881400hg38UCSC Ensembl
chr15:101417906..101421605hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178477
Samples
Known GenesALDH1A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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