A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061594



Internal ID20628634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47103166..47155282hg38UCSC Ensembl
chr1:47568838..47620954hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3852117
hg1952117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316080
Supporting Variants
Samples
Known GenesCYP4A22, CYP4Z1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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