A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334249



Internal ID20867432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190029217..190087299hg38UCSC Ensembl
chr1:189998347..190056429hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3858083
hg1958083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18055167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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