A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362370



Internal ID22588039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10194734..10197380hg38UCSC Ensembl
chr1:10254792..10257438hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382647
hg192647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362370
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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