A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3483596



Internal ID19071237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684762..109697544hg38UCSC Ensembl
Innerchr1:110227384..110240166hg19UCSC Ensembl
Innerchr1:110028907..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3812783
hg1912783
hg1812783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008891
Supporting Variants
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3483596
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