A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513514



Internal ID22571469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42925176..42940042hg38UCSC Ensembl
chr9:44031077..44045943hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3814867
hg1914867
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513514
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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