A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688767



Internal ID18640362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28847172..29154878hg38UCSC Ensembl
Innerchr9:28847170..29154876hg19UCSC Ensembl
Innerchr9:28837170..29144876hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38307707
hg19307707
hg18307707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020807
Supporting Variants
Samples
Known GenesLINGO2, MIR873, MIR876
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688767
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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