A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532271



Internal ID20905632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58663696..58672609hg38UCSC Ensembl
chr17:56741057..56749970hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg388914
hg198914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036316
Samples
Known GenesTEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer