A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381447



Internal ID21039000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140542253..140542740hg38UCSC Ensembl
chr4:141463407..141463894hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108121
Samples
Known GenesELMOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381447
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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