A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442269



Internal ID22500139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10060061..10060061hg38UCSC Ensembl
chr8:9917571..9917571hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952862
Supporting Variants
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442269
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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