A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577679



Internal ID16365088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76393396..76407764hg38UCSC Ensembl
Innerchr18:74105352..74119720hg19UCSC Ensembl
Innerchr18:72234340..72248708hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3814369
hg1914369
hg1814369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6073n54
Supporting Variantsnssv887520
Samples
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577679
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