A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386112



Internal ID21043665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64275617..64277426hg38UCSC Ensembl
chr4:65141335..65143144hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381810
hg191810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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