A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011725



Internal ID19100943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21745401..21762936hg38UCSC Ensembl
Innerchr3:21786893..21804428hg19UCSC Ensembl
Innerchr3:21761897..21779432hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3817536
hg1917536
hg1817536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4691n100
Supporting Variantsnssv3593155, nssv3593154
Samples
Known GenesZNF385D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011725
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