A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467823



Internal ID22525715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98622891..98624145hg38UCSC Ensembl
chr12:99016669..99017923hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851670
Supporting Variants
Samples
Known GenesIKBIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467823
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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