A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384450



Internal ID21042003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155568021..155568521hg38UCSC Ensembl
chr4:156489173..156489673hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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