A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577691



Internal ID16365100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76697012..76763414hg38UCSC Ensembl
Innerchr18:74408968..74475370hg19UCSC Ensembl
Innerchr18:72537956..72604358hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3866403
hg1966403
hg1866403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6077n54
Supporting Variantsnssv887539
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577691
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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