A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689471



Internal ID18987752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61605421..61961244hg38UCSC Ensembl
Innerchr8:62517980..62873803hg19UCSC Ensembl
Innerchr8:62680534..63036357hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38355824
hg19355824
hg18355824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015216
Supporting Variants
Samples
Known GenesASPH, MIR4470
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689471
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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