A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390637



Internal ID21048190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71604005..71650721hg38UCSC Ensembl
chr4:72469722..72516438hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3846717
hg1946717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390637
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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