A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523585



Internal ID20896946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49233679..49271709hg38UCSC Ensembl
chr17:47311041..47349071hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3838031
hg1938031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036115
Samples
Known GenesFLJ40194
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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