A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1090131



Internal ID15943317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90181390..90183138hg38UCSC Ensembl
Innerchr7:89810704..89812452hg19UCSC Ensembl
Innerchr7:89648640..89650388hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381749
hg191749
hg181749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607783
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)nssv1090131
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