A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504241



Internal ID20877502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48888468..48888803hg38UCSC Ensembl
chr15:49180665..49181000hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190569
Samples
Known GenesSHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504241
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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