A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035035



Internal ID18777566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123883276..124008232hg38UCSC Ensembl
Innerchr8:124895516..125020472hg19UCSC Ensembl
Innerchr8:124964697..125089653hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38124957
hg19124957
hg18124957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7308n100
Supporting Variantsnssv3691500
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)nsv1035035
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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