A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329362



Internal ID20862514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15188988..15224213hg38UCSC Ensembl
chr1:15515484..15550709hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3835226
hg1935226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200428
Samples
Known GenesTMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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