A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060500



Internal ID20627540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42806229..42809909hg38UCSC Ensembl
chr1:43271900..43275580hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383681
hg193681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321849
Supporting Variants
Samples
Known GenesCCDC23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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