A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333505



Internal ID20866683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184640093..184645473hg38UCSC Ensembl
chr1:184609227..184614607hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385381
hg195381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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