A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380742



Internal ID21038295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47591646..47592272hg38UCSC Ensembl
chr4:47593663..47594289hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117227
Samples
Known GenesATP10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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