A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394325



Internal ID21051878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104777665..104778395hg38UCSC Ensembl
chr4:105698822..105699552hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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