A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685543



Internal ID18637138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28511580..28577696hg38UCSC Ensembl
Innerchr8:28369097..28435213hg19UCSC Ensembl
Innerchr8:28425016..28491132hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3866117
hg1966117
hg1866117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030130
Supporting Variants
Samples
Known GenesFZD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685543
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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