A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048345



Internal ID19137564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:120196924..120275786hg38UCSC Ensembl
Innerchr9:122959202..123038064hg19UCSC Ensembl
Innerchr9:121999023..122077885hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3878863
hg1978863
hg1878863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759823
Samples
Known GenesMIR147A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048345
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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