A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200934



Internal ID20767974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157096695..157097247hg38UCSC Ensembl
chr1:157066487..157067039hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334077
Supporting Variants
Samples
Known GenesETV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200934
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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