A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1049519



Internal ID15902705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:16884786..16892181hg38UCSC Ensembl
Innerchr6:16885017..16892412hg19UCSC Ensembl
Innerchr6:16992996..17000391hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387396
hg197396
hg187396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601016
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)nssv1049519
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