A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177903



Internal ID20744943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1564993..1571034hg38UCSC Ensembl
chr17:1468287..1474328hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg386042
hg196042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512906
Supporting Variants
Samples
Known GenesSLC43A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00163


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