A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453417



Internal ID22511291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111811525..111815095hg38UCSC Ensembl
chr12:112249329..112252899hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg383571
hg193571
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453417
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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