A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498957



Internal ID20872172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14188901..14190900hg38UCSC Ensembl
chr17:14092218..14094217hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192578
Samples
Known GenesCOX10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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