A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317565



Internal ID20850652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223504086..223513083hg38UCSC Ensembl
chr1:223677428..223686425hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg388998
hg198998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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