A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575290



Internal ID21767333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107729974..107730221hg38UCSC Ensembl
chr7:107370419..107370666hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575290
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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