A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350679



Internal ID22576348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109378607..109378748hg38UCSC Ensembl
chr1:109921229..109921370hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874270
Supporting Variants
Samples
Known GenesSORT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350679
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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