A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017774



Internal ID19106991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5378269..5396960hg38UCSC Ensembl
Innerchr9:5378269..5396960hg19UCSC Ensembl
Innerchr9:5368269..5386960hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3818692
hg1918692
hg1818692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7385n100
Supporting Variantsnssv3692418
Samples
Known GenesPLGRKT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017774
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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