A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695149



Internal ID18646744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113092097..113105232hg38UCSC Ensembl
Innerchr9:115854377..115867512hg19UCSC Ensembl
Innerchr9:114894198..114907333hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3813136
hg1913136
hg1813136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043365
Supporting Variants
Samples
Known GenesFAM225B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695149
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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