A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359592



Internal ID22585261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156265246..156265246hg38UCSC Ensembl
chr1:156235037..156235037hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954505
Supporting Variants
Samples
Known GenesSMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359592
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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