A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008010



Internal ID19097229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91627676hg38UCSC Ensembl
Innerchr2:91618895..91815702hg19UCSC Ensembl
Innerchr2:90982622..91179429hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38201151
hg19196808
hg18196808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3990n100
Supporting Variantsnssv3579422, nssv3579426, nssv3579427, nssv3579425, nssv3579421, nssv3579424, nssv3579423
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)nsv1008010
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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