A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470704



Internal ID22528595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101787418..101814246hg38UCSC Ensembl
chr15:102327621..102354449hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3826829
hg1926829
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876407
Supporting Variants
Samples
Known GenesOR4F6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470704
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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