A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360382



Internal ID22586051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7160227..7160227hg38UCSC Ensembl
chr12:7312823..7312823hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360382
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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