A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980705



Internal ID20547745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131111657..131245370hg38UCSC Ensembl
chr10:132909920..133043633hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38133714
hg19133714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439963
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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