A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362505



Internal ID21020058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8952480..8984287hg38UCSC Ensembl
chr4:8954206..8986013hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3831808
hg1931808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5147n223
Supporting Variantsnssv18122477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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