A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004355



Internal ID19093572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91601674hg38UCSC Ensembl
Innerchr2:91618895..91789700hg19UCSC Ensembl
Innerchr2:90982622..91153427hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38175149
hg19170806
hg18170806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3990n100
Supporting Variantsnssv3579407, nssv3579408
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)nsv1004355
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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