A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201952



Internal ID20768993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166240601..166243200hg38UCSC Ensembl
chr1:166209838..166212437hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00367


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