A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571423



Internal ID21763466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116337236..116337236hg38UCSC Ensembl
chr7:115977290..115977290hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571423
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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