A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359337



Internal ID21016890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10370501..10517500hg38UCSC Ensembl
chr4:10372125..10519124hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38147000
hg19147000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209458
Samples
Known GenesCLNK, ZNF518B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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