A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364345



Internal ID22590014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95297256..95298343hg38UCSC Ensembl
chr10:97057013..97058100hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364345
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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