A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023617



Internal ID19112834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94249727..94272186hg38UCSC Ensembl
Innerchr8:95261955..95284414hg19UCSC Ensembl
Innerchr8:95331131..95353590hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3822460
hg1922460
hg1822460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7270n100
Supporting Variantsnssv3689725
Samples
Known GenesGEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023617
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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