A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695146



Internal ID18646741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113092059..113121461hg38UCSC Ensembl
Innerchr9:115854339..115883741hg19UCSC Ensembl
Innerchr9:114894160..114923562hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3829403
hg1929403
hg1829403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042807
Supporting Variants
Samples
Known GenesFAM225A, FAM225B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695146
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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