A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612713



Internal ID16400122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142763851..142775790hg38UCSC Ensembl
Innerchr8:143845269..143857208hg19UCSC Ensembl
Innerchr8:143842271..143854210hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3811940
hg1911940
hg1811940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1124935
Samples
Known GenesLYNX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612713
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