A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452009



Internal ID22509881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1382943..1401341hg38UCSC Ensembl
chr1:1318323..1336721hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3818399
hg1918399
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828185
Supporting Variants
Samples
Known GenesCCNL2, LOC148413
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452009
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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