A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059182



Internal ID20626222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227930652..227942112hg38UCSC Ensembl
chr1:228118353..228129813hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3811461
hg1911461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326104
Supporting Variants
Samples
Known GenesMIR5008, WNT9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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