A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555000



Internal ID20928089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14371662..14372255hg38UCSC Ensembl
chr21:15743983..15744576hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068616
Samples
Known GenesHSPA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555000
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