A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190764



Internal ID20757804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109701701..109828300hg38UCSC Ensembl
chr13:110354048..110480647hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38126600
hg19126600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487192
Supporting Variants
Samples
Known GenesIRS2, LINC00676
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190764
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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