A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201752



Internal ID20768792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183575202..183585358hg38UCSC Ensembl
chr1:183544337..183554493hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3810157
hg1910157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327543
Supporting Variants
Samples
Known GenesNCF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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