A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052898



Internal ID20619938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14861147..14866455hg38UCSC Ensembl
chr1:15187643..15192951hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg385309
hg195309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318462
Supporting Variants
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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