A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203501



Internal ID20770541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27370335..27376901hg38UCSC Ensembl
chr1:27696826..27703393hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386567
hg196568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316101
Supporting Variants
Samples
Known GenesFCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203501
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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