A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466948



Internal ID22524839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96985470..96986969hg38UCSC Ensembl
chr12:97379248..97380747hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466948
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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