A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357315



Internal ID22582984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231556867..231559319hg38UCSC Ensembl
chr1:231692613..231695065hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382453
hg192453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879458
Supporting Variants
Samples
Known GenesTSNAX, TSNAX-DISC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357315
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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