A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385234



Internal ID21042787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71856102..71856534hg38UCSC Ensembl
chr4:72721819..72722251hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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