A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024843



Internal ID18767374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17813558..17869789hg38UCSC Ensembl
Innerchr8:17671067..17727298hg19UCSC Ensembl
Innerchr8:17715347..17771578hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3856232
hg1956232
hg1856232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760464
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)nsv1024843
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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