A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380923



Internal ID21038476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102052394..102113549hg38UCSC Ensembl
chr4:102973551..103034706hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3861156
hg1961156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106214
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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