A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385743



Internal ID21043296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168161497..168168898hg38UCSC Ensembl
chr4:169082648..169090049hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg387402
hg197402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115326
Samples
Known GenesANXA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385743
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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