A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002403



Internal ID19091620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45103892..45124910hg38UCSC Ensembl
Innerchr2:45331031..45352049hg19UCSC Ensembl
Innerchr2:45184535..45205553hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3821019
hg1921019
hg1821019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3803n100
Supporting Variantsnssv3581607, nssv3725993, nssv3581606, nssv3581605
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)nsv1002403
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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