A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465525



Internal ID22523414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97531213..97535071hg38UCSC Ensembl
chr12:97924991..97928849hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854480
Supporting Variants
Samples
Known GenesRMST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465525
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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