A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200414



Internal ID20767454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151325067..151336043hg38UCSC Ensembl
chr1:151297543..151308519hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3810977
hg1910977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319505
Supporting Variants
Samples
Known GenesPI4KB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200414
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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