A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507667



Internal ID20880961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15644939..15652250hg38UCSC Ensembl
chr17:15548253..15555564hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg387312
hg197312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033925
Samples
Known GenesTRIM16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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