A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1063662



Internal ID15570162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69948540..70030259hg38UCSC Ensembl
Innerchr6:70658432..70740151hg19UCSC Ensembl
Innerchr6:70715153..70796872hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3881720
hg1981720
hg1881720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603637
Supporting Variants
Samples
Known GenesCOL19A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1063662
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