A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526801



Internal ID21851158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244428584..244428664hg38UCSC Ensembl
chr1:244591886..244591966hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983165
Supporting Variants
Samples
Known GenesADSS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526801
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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