A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202118



Internal ID20769158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9679096..9685503hg38UCSC Ensembl
chr1:9739154..9745561hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg386408
hg196408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319735
Supporting Variants
Samples
Known GenesPIK3CD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202118
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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