A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567453



Internal ID21759496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138920151..138920151hg38UCSC Ensembl
chr7:138604897..138604897hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065078
Supporting Variants
Samples
Known GenesKIAA1549
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567453
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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