A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029766



Internal ID19118985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6437020..6523605hg38UCSC Ensembl
Innerchr9:6437020..6523605hg19UCSC Ensembl
Innerchr9:6427020..6513605hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3886586
hg1986586
hg1886586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689081
Samples
Known GenesUHRF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029766
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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