A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039528



Internal ID19128747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104152475..104219309hg38UCSC Ensembl
Innerchr9:106914756..106981590hg19UCSC Ensembl
Innerchr9:105954577..106021411hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3866835
hg1966835
hg1866835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697633
Samples
Known GenesMIR6130
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039528
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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