A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611118



Internal ID20984189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157261953..157265632hg38UCSC Ensembl
chr6:157614001..157617680hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383680
hg193680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611118
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