A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999806



Internal ID19159342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91602037hg38UCSC Ensembl
Innerchr2:91618895..91790063hg19UCSC Ensembl
Innerchr2:90982622..91153790hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38175512
hg19171169
hg18171169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3990n100
Supporting Variantsnssv3579409
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)nsv999806
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