A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465849



Internal ID22523738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161821496..161929487hg38UCSC Ensembl
chr1:161791286..161899277hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38107992
hg19107992
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828503
Supporting Variants
Samples
Known GenesATF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465849
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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