A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025796



Internal ID18768328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80548436..80584622hg38UCSC Ensembl
Innerchr5:79844255..79880441hg19UCSC Ensembl
Innerchr5:79880011..79916197hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3836187
hg1936187
hg1836187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5705n100
Supporting Variantsnssv3639070, nssv3639071
Samples
Known GenesANKRD34B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025796
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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