A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501981



Internal ID20875221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15555401..15575900hg38UCSC Ensembl
chr17:15458715..15479214hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3820500
hg1920500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188186
Samples
Known GenesCDRT1, TVP23C, TVP23C-CDRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501981
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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