A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524209



Internal ID20897570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58581079..58591284hg38UCSC Ensembl
chr17:56658440..56668645hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810206
hg1910206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036309
Samples
Known GenesTEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524209
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