A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335239



Internal ID20868431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51485945..51501353hg38UCSC Ensembl
chr1:51951617..51967025hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3815409
hg1915409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061990
Samples
Known GenesEPS15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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