A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460471



Internal ID22518354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3603431..3608933hg38UCSC Ensembl
chr12:3712597..3718099hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg385503
hg195503
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460471
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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