A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384407



Internal ID21041960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46803099..46804489hg38UCSC Ensembl
chr4:46805116..46806506hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117162
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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