A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757366



Internal ID18708961
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 StatusS
Merged Variantsnsv1033617
Supporting Variants
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)nssv3757366
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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