A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356688



Internal ID22582357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29189159..29189290hg38UCSC Ensembl
chr1:29515671..29515802hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356688
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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