A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036586



Internal ID18779117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113356622..113374713hg38UCSC Ensembl
Innerchr9:116118902..116136993hg19UCSC Ensembl
Innerchr9:115158723..115176814hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3818092
hg1918092
hg1818092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759813, nssv3695152, nssv3695153
Samples
Known GenesBSPRY, HDHD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036586
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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