A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022398



Internal ID19111616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:310716..381630hg38UCSC Ensembl
Innerchr8:260716..331630hg19UCSC Ensembl
Innerchr8:250716..321630hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3870915
hg1970915
hg1870915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6793n100
Supporting Variantsnssv3674923
Samples
Known GenesFAM87A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022398
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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