A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379987



Internal ID21037540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16176801..16180000hg38UCSC Ensembl
chr5:16176910..16180109hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215949
Samples
Known GenesMARCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379987
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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