A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075614



Internal ID15582114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163414144..163415657hg38UCSC Ensembl
Innerchr6:163835176..163836689hg19UCSC Ensembl
Innerchr6:163755166..163756679hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381514
hg191514
hg181514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605207
Supporting Variants
Samples
Known GenesQKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075614
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