A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510312



Internal ID22568262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98214333..98218851hg38UCSC Ensembl
chr8:99226561..99231079hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg384519
hg194519
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854006
Supporting Variants
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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