A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509737



Internal ID20883048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15730401..15771000hg38UCSC Ensembl
chr17:15633715..15674314hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3840600
hg1940600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3008n223
Supporting Variantsnssv18190886
Samples
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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