A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317294



Internal ID20850378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161951901..161954300hg38UCSC Ensembl
chr1:161921691..161924090hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053297
Samples
Known GenesATF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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