A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357962



Internal ID22583631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151191408..151191711hg38UCSC Ensembl
chr1:151163884..151164187hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357962
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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