A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380162



Internal ID21037715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45078655..45082803hg38UCSC Ensembl
chr4:45080672..45084820hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg384149
hg194149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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