A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369532



Internal ID22595201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244918718..244918817hg38UCSC Ensembl
chr1:245082020..245082119hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369532
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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