A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460237



Internal ID22518123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180731416..180754095hg38UCSC Ensembl
chr1:180700552..180723231hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3822680
hg1922680
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828435
Supporting Variants
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460237
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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