A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372245



Internal ID22597914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95539884..95540424hg38UCSC Ensembl
chr13:96192138..96192678hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947232
Supporting Variants
Samples
Known GenesCLDN10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372245
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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