A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386942



Internal ID21044495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145910058..145911211hg38UCSC Ensembl
chr4:146831210..146832363hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg381154
hg191154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108909
Samples
Known GenesZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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