A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202136



Internal ID20769176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9896654..9897940hg38UCSC Ensembl
chr1:9956712..9957998hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322116
Supporting Variants
Samples
Known GenesCTNNBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202136
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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