A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500152



Internal ID20873377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15515901..15593300hg38UCSC Ensembl
chr17:15419215..15496614hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3877400
hg1977400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033902
Samples
Known GenesCDRT1, TVP23C, TVP23C-CDRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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