A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976602



Internal ID16270558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149550714..149553300hg38UCSC Ensembl
Innerchr3:149268501..149271087hg19UCSC Ensembl
Innerchr3:150751191..150753777hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382587
hg192587
hg182587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592016
Supporting Variants
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976602
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