A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466497



Internal ID22524389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:247490365..247491964hg38UCSC Ensembl
chr1:247653667..247655266hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829603
Supporting Variants
Samples
Known GenesOR2W5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466497
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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