A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570667



Internal ID21762710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93140116..93140116hg38UCSC Ensembl
chr7:92769429..92769429hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062490
Supporting Variants
Samples
Known GenesSAMD9L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570667
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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