A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528588



Internal ID21852945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19294097..19294158hg38UCSC Ensembl
chr1:19620591..19620652hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982071
Supporting Variants
Samples
Known GenesLOC100506730
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528588
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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