A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200729



Internal ID20767769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:247235901..247241400hg38UCSC Ensembl
chr1:247399203..247404702hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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