A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512574



Internal ID22570528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27274047..27289398hg38UCSC Ensembl
chr9:27274045..27289396hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3815352
hg1915352
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849955
Supporting Variants
Samples
Known GenesEQTN, LINC00032
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512574
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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