A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1068396



Internal ID15921582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:90295770..90296753hg38UCSC Ensembl
Innerchr6:91005489..91006472hg19UCSC Ensembl
Innerchr6:91062210..91063193hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38984
hg19984
hg18984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604129
Supporting Variants
Samples
Known GenesBACH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1068396
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