A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072095



Internal ID15925281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113901546..113903811hg38UCSC Ensembl
Innerchr6:114222710..114224975hg19UCSC Ensembl
Innerchr6:114329403..114331668hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382266
hg192266
hg182266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604533
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072095
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