A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609186



Internal ID16396595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156594543..156611368hg38UCSC Ensembl
Innerchr7:156387237..156404062hg19UCSC Ensembl
Innerchr7:156079998..156096823hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3816826
hg1916826
hg1816826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11759n54
Supporting Variantsnssv1100470, nssv1100471
Samples
Known GenesLINC01006
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609186
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer