A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366830



Internal ID21024383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:213369..386896hg38UCSC Ensembl
chr4:207158..380685hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38173528
hg19173528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212855
Samples
Known GenesZNF141, ZNF732, ZNF876P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366830
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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