A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028148



Internal ID18770679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85398341..85640901hg38UCSC Ensembl
Innerchr8:86310570..86553130hg19UCSC Ensembl
Innerchr8:86497822..86740382hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38242561
hg19242561
hg18242561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689645
Samples
Known GenesCA2, CA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028148
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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