A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690553



Internal ID18988834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12008565..12110043hg38UCSC Ensembl
Innerchr9:12008565..12110043hg19UCSC Ensembl
Innerchr9:11998565..12100043hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38101479
hg19101479
hg18101479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034783
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690553
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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