A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016426



Internal ID19105645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53042643..53080343hg38UCSC Ensembl
Innerchr8:53955203..53992903hg19UCSC Ensembl
Innerchr8:54117756..54155456hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3837701
hg1937701
hg1837701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7224n100
Supporting Variantsnssv3687532, nssv3687529, nssv3687533, nssv3687530, nssv3687531, nssv3687534
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)nsv1016426
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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