A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577971



Internal ID16018694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:80197495..80257297hg38UCSC Ensembl
Innerchr18:77955378..78015180hg19UCSC Ensembl
Innerchr18:76056369..76116152hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3859803
hg1959803
hg1859784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv890323
Samples
Known GenesPARD6G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577971
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