A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020650



Internal ID19109869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64493516..64898828hg38UCSC Ensembl
Innerchr9:69505934..69911246hg19UCSC Ensembl
Innerchr9:68795754..69201066hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38405313
hg19405313
hg18405313
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7657n100
Supporting Variantsnssv3696144
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020650
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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