A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363171



Internal ID21020724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30116843..30123916hg38UCSC Ensembl
chr4:30118465..30125538hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg387074
hg197074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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