A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195969



Internal ID20763009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44588661..44604104hg38UCSC Ensembl
chr17:42666029..42681472hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3815444
hg1915444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195969
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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