A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749129



Internal ID21385085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111319992..111321917hg38UCSC Ensembl
chr6:111641195..111643120hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381926
hg191926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434725
Supporting Variants
SamplesBTQ038
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749129
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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