A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201526



Internal ID20768567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150746712..150796893hg38UCSC Ensembl
chr1:150719188..150769369hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3850182
hg1950182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321317
Supporting Variants
Samples
Known GenesCTSK, CTSS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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