A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035258



Internal ID19124477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104050851..104090136hg38UCSC Ensembl
Innerchr9:106813132..106852417hg19UCSC Ensembl
Innerchr9:105852953..105892238hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3839286
hg1939286
hg1839286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7695n100
Supporting Variantsnssv3697625, nssv3697626, nssv3697627, nssv3697630, nssv3697628, nssv3697629
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)nsv1035258
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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