A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200925



Internal ID20767965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156642676..156693021hg38UCSC Ensembl
chr1:156612468..156662813hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3850346
hg1950346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321357
Supporting Variants
Samples
Known GenesBCAN, NES
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200925
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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