A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512677



Internal ID22570631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2899531..2900688hg38UCSC Ensembl
chr9:2899531..2900688hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381158
hg191158
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512677
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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