A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352178



Internal ID22577847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157760658..157760717hg38UCSC Ensembl
chr1:157730448..157730507hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886543
Supporting Variants
Samples
Known GenesFCRL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352178
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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