A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323879



Internal ID20857002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205086238..205087198hg38UCSC Ensembl
chr1:205055366..205056326hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201856
Samples
Known GenesRBBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323879
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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