A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603520



Internal ID21795567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27819361..27819361hg38UCSC Ensembl
chr12:27972294..27972294hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603520
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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