A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950155



Internal ID16952342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32005124..32037723hg38UCSC Ensembl
Outerchr6:31972901..32005500hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3832600
hg1932600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997427
SamplesBILGI_BIOE
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950155
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