A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381504



Internal ID22439374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70600774..70600864hg38UCSC Ensembl
chr1:71066457..71066547hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381504
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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