A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335191



Internal ID20868383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155938940..155945806hg38UCSC Ensembl
chr1:155908731..155915597hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg386867
hg196867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200917
Samples
Known GenesRXFP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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