A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350137



Internal ID22575806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95271782..95290816hg38UCSC Ensembl
chr10:97031539..97050573hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3819035
hg1919035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910099
Supporting Variants
Samples
Known GenesPDLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350137
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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