A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690674



Internal ID18988955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18270457..18295316hg38UCSC Ensembl
Innerchr9:18270455..18295314hg19UCSC Ensembl
Innerchr9:18260455..18285314hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3824860
hg1924860
hg1824860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020662
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)nssv3690674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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