A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630535



Internal ID21822582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75777152..75777152hg38UCSC Ensembl
chr17:73773233..73773233hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081165
Supporting Variants
Samples
Known GenesH3F3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630535
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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