A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014694



Internal ID19103911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84868298..84910178hg38UCSC Ensembl
Innerchr3:84917449..84959329hg19UCSC Ensembl
Innerchr3:85000139..85042019hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3841881
hg1941881
hg1841881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596265
Samples
Known GenesLINC00971
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014694
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