A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363182



Internal ID22588851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2348742..2348807hg38UCSC Ensembl
chr1:2280181..2280246hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868045
Supporting Variants
Samples
Known GenesMORN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363182
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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