A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500608



Internal ID20873836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12781496..12782989hg38UCSC Ensembl
chr17:12684813..12686306hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381494
hg191494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034213
Samples
Known GenesLOC100128006
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500608
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