A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982997



Internal ID20550037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68143962..68145231hg38UCSC Ensembl
chr10:69903719..69904988hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381270
hg191270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439280
Supporting Variants
Samples
Known GenesMYPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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