A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020573



Internal ID19109792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64555437..64886202hg38UCSC Ensembl
Innerchr9:69567855..69898620hg19UCSC Ensembl
Innerchr9:68857675..69188440hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38330766
hg19330766
hg18330766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7659n100
Supporting Variantsnssv3696155
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)nsv1020573
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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