A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1120523



Internal ID15973709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123915471..123976027hg38UCSC Ensembl
Innerchr8:124927711..124988267hg19UCSC Ensembl
Innerchr8:124996892..125057448hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3860557
hg1960557
hg1860557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612143
Supporting Variants
Samples
Known GenesFER1L6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1120523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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