A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437823



Internal ID22495693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128865326..128865326hg38UCSC Ensembl
chr9:131627605..131627605hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966989
Supporting Variants
Samples
Known GenesCCBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437823
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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