A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072366



Internal ID15925552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123271188..123273399hg38UCSC Ensembl
Innerchr6:123592333..123594544hg19UCSC Ensembl
Innerchr6:123634032..123636243hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382212
hg192212
hg182212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604578
Supporting Variants
Samples
Known GenesTRDN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072366
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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