A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324058



Internal ID20857182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33879971..33881709hg38UCSC Ensembl
chr1:34345572..34347310hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381739
hg191739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060985
Samples
Known GenesCSMD2, LOC402779
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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