A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011073



Internal ID19100290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77247704..77334274hg38UCSC Ensembl
Innerchr4:78168857..78255427hg19UCSC Ensembl
Innerchr4:78387881..78474451hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3886571
hg1986571
hg1886571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5323n100
Supporting Variantsnssv3633852, nssv3633849, nssv3633851, nssv3633850
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)nsv1011073
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