A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955334



Internal ID16957521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126101258..126137757hg38UCSC Ensembl
Outerchr3:125820101..125856600hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3836500
hg1936500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001451
SamplesBILGI_BIOE
Known GenesALDH1L1, ALDH1L1-AS1, SLC41A3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955334
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