A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701946



Internal ID21223776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75383648..75383737hg38UCSC Ensembl
chr9:77998564..77998653hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819974
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701946
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.484375


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