A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386880



Internal ID21044433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112818639..112820467hg38UCSC Ensembl
chr4:113739795..113741623hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381829
hg191829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105645
Samples
Known GenesANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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