A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010340



Internal ID19099557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:711922..948729hg38UCSC Ensembl
Innerchr2:711922..944415hg19UCSC Ensembl
Innerchr2:701922..934415hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38236808
hg19232494
hg18232494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3700n100
Supporting Variantsnssv3726655
Samples
Known GenesLINC01115
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010340
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