A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685544



Internal ID18637139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28516920..28569458hg38UCSC Ensembl
Innerchr8:28374437..28426975hg19UCSC Ensembl
Innerchr8:28430356..28482894hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3852539
hg1952539
hg1852539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021367
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)nssv3685544
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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