A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033851



Internal ID19123072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53047072..53079271hg38UCSC Ensembl
Innerchr8:53959632..53991831hg19UCSC Ensembl
Innerchr8:54122185..54154384hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3832200
hg1932200
hg1832200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7224n100
Supporting Variantsnssv3687536, nssv3687535, nssv3687537
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033851
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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