A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356016



Internal ID22581685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25376348..25379174hg38UCSC Ensembl
chr1:25702839..25705665hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382827
hg192827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873119
Supporting Variants
Samples
Known GenesRHCE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356016
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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