A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697549



Internal ID18649144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91590379..91893734hg38UCSC Ensembl
Innerchr9:94352661..94656016hg19UCSC Ensembl
Innerchr9:93392482..93695837hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38303356
hg19303356
hg18303356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045332
Supporting Variants
Samples
Known GenesMIR3910-1, MIR3910-2, ROR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697549
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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