A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571108



Internal ID21763151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155590320..155590320hg38UCSC Ensembl
chr7:155383014..155383014hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571108
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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