A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380068



Internal ID21037621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61427488..61428135hg38UCSC Ensembl
chr4:62293206..62293853hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380068
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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