A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369519



Internal ID22595188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110770069..110772142hg38UCSC Ensembl
chr1:111312691..111314764hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382074
hg192074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872275
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369519
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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