A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616932



Internal ID21808979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100201864..100203273hg38UCSC Ensembl
chr13:100854118..100855527hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381410
hg191410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023156
Supporting Variants
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616932
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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