A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200939



Internal ID20767979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15785468..15790332hg38UCSC Ensembl
chr1:16111963..16116827hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384865
hg194865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320213
Supporting Variants
Samples
Known GenesFBLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200939
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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