A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357454



Internal ID22583123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32904514..32904514hg38UCSC Ensembl
chr12:33057448..33057448hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976847
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357454
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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