A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999106



Internal ID19158642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34845678hg38UCSC Ensembl
Innerchr4:34761520..34847300hg19UCSC Ensembl
Innerchr4:34437915..34523695hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3885781
hg1985781
hg1885781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5165n100
Supporting Variantsnssv3620676, nssv3620677, nssv3620678
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)nsv999106
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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