A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683821



Internal ID21205678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133203094..133203201hg38UCSC Ensembl
chr10:135016598..135016705hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788822
Supporting Variants
Samples
Known GenesKNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683821
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.288462


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