A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034118



Internal ID18776652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17876103..17916258hg38UCSC Ensembl
Innerchr8:17733612..17773767hg19UCSC Ensembl
Innerchr8:17777892..17818047hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3840156
hg1940156
hg1840156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760465
Samples
Known GenesFGL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034118
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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