A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200538



Internal ID20767578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155780091..155782951hg38UCSC Ensembl
chr1:155749882..155752742hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382861
hg192861
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318255
Supporting Variants
Samples
Known GenesGON4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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