A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203190



Internal ID20770230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9397008..9459851hg38UCSC Ensembl
chr1:9457067..9519910hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3862844
hg1962844
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335314
Supporting Variants
Samples
Known GenesLOC100506022
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203190
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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