A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351231



Internal ID22576900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4259458..4259458hg38UCSC Ensembl
chr12:4368624..4368624hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351231
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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