A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007148



Internal ID19096366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:82442276..82535031hg38UCSC Ensembl
Innerchr1:82907959..83000714hg19UCSC Ensembl
Innerchr1:82680547..82773302hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3892756
hg1992756
hg1892756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv205n100
Supporting Variantsnssv3475051
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)nsv1007148
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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