A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997336



Internal ID19156874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:137933709..137948780hg38UCSC Ensembl
Innerchr3:137652551..137667622hg19UCSC Ensembl
Innerchr3:139135241..139150312hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3815072
hg1915072
hg1815072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3608323
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997336
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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