A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367128



Internal ID21024681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157097641..157100111hg38UCSC Ensembl
chr3:156815430..156817900hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg382471
hg192471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096773
Samples
Known GenesLINC00880, LINC00881
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367128
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