A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319460



Internal ID20852555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24014499..24019411hg38UCSC Ensembl
chr1:24340989..24345901hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384913
hg194913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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