A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333618



Internal ID20866798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87397104..87397829hg38UCSC Ensembl
chr1:87862787..87863512hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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