A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506255



Internal ID20879533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57581285..57611667hg38UCSC Ensembl
chr15:57873483..57903865hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3830383
hg1930383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178667
Samples
Known GenesGCOM1, MYZAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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