A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334546



Internal ID20867733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155679901..155755500hg38UCSC Ensembl
chr1:155649692..155725291hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3875600
hg1975600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200534
Samples
Known GenesDAP3, GON4L, MSTO2P, YY1AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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