A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691549



Internal ID18989830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132769940..132856429hg38UCSC Ensembl
Innerchr8:133782186..133868674hg19UCSC Ensembl
Innerchr8:133851368..133937856hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3886490
hg1986489
hg1886489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027570
Supporting Variants
Samples
Known GenesPHF20L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691549
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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