A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035977



Internal ID18778508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73870179..73906608hg38UCSC Ensembl
Innerchr11:73581224..73617653hg19UCSC Ensembl
Innerchr11:73258872..73295301hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3836430
hg1936430
hg1836430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503210
Samples
Known GenesCOA4, PAAF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035977
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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