A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361806



Internal ID21019359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27821738..27822437hg38UCSC Ensembl
chr4:27823360..27824059hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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