A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364380



Internal ID22590049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70269236..70269590hg38UCSC Ensembl
chr10:72028992..72029346hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913292
Supporting Variants
Samples
Known GenesNPFFR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364380
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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