A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056702



Internal ID20623743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202854058..202866940hg38UCSC Ensembl
chr1:202823186..202836068hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3812883
hg1912883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317097
Supporting Variants
Samples
Known GenesLOC148709
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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