A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033617



Internal ID18776150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123883276..124000543hg38UCSC Ensembl
Innerchr8:124895516..125012783hg19UCSC Ensembl
Innerchr8:124964697..125081964hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38117268
hg19117268
hg18117268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7308n100
Supporting Variantsnssv3757366
Samples
Known GenesFER1L6, FER1L6-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033617
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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