A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689695



Internal ID18987976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88828949..88939682hg38UCSC Ensembl
Innerchr8:89841178..89951911hg19UCSC Ensembl
Innerchr8:89910294..90021027hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38110734
hg19110734
hg18110734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029213
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)nssv3689695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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