A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051246



Internal ID20618286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119172193..119179881hg38UCSC Ensembl
chr1:119714816..119722504hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg387689
hg197689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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