A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997260



Internal ID19156798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:198583115..198619566hg38UCSC Ensembl
Innerchr1:198552245..198588696hg19UCSC Ensembl
Innerchr1:196818868..196855319hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3836452
hg1936452
hg1836452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3483873
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)nsv997260
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