A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931264



Internal ID21351333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122124329..122124412hg38UCSC Ensembl
chr12:122608876..122608959hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15182179
SamplesHG002
Known GenesMLXIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931264
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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