A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977177



Internal ID20544217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100995294..100997795hg38UCSC Ensembl
chr10:102755051..102757552hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437455
Supporting Variants
Samples
Known GenesLZTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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