A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023866



Internal ID19113083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95261027..95294150hg38UCSC Ensembl
Innerchr8:96273255..96306378hg19UCSC Ensembl
Innerchr8:96342431..96375554hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833124
hg1933124
hg1833124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689733
Samples
Known GenesC8orf37, LOC100616530
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023866
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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