A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322168



Internal ID20855278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28055259..28075201hg38UCSC Ensembl
chr1:28381770..28401712hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3819943
hg1919943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060696
Samples
Known GenesEYA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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