A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615965



Internal ID20989036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111818643..111819354hg38UCSC Ensembl
chr6:112139846..112140557hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135429
Samples
Known GenesFYN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615965
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