A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510640



Internal ID22568591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106977244..106979843hg38UCSC Ensembl
chr9:109739525..109742124hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864995
Supporting Variants
Samples
Known GenesMIR548Q, ZNF462
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510640
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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