A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017148



Internal ID19106365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131913210..131940146hg38UCSC Ensembl
Innerchr8:132925457..132952393hg19UCSC Ensembl
Innerchr8:132994639..133021575hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3826937
hg1926937
hg1826937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691538
Samples
Known GenesEFR3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017148
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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