A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508865



Internal ID20882169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15731001..15774100hg38UCSC Ensembl
chr17:15634315..15677414hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3843100
hg1943100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3008n223
Supporting Variantsnssv18184430
Samples
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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