A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027042



Internal ID19116261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9208635..9300048hg38UCSC Ensembl
Innerchr9:9208635..9300048hg19UCSC Ensembl
Innerchr9:9198635..9290048hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3891414
hg1991414
hg1891414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758123
Samples
Known GenesPTPRD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027042
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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