A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018542



Internal ID19107759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53047072..53080343hg38UCSC Ensembl
Innerchr8:53959632..53992903hg19UCSC Ensembl
Innerchr8:54122185..54155456hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3833272
hg1933272
hg1833272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7224n100
Supporting Variantsnssv3688658, nssv3688661, nssv3688653, nssv3688654, nssv3687541, nssv3687542, nssv3687540, nssv3688650, nssv3688655, nssv3688652, nssv3688657, nssv3688656, nssv3688660, nssv3687539, nssv3688659, nssv3688651, nssv3687538
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)nsv1018542
Frequency
Sample Size11257
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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