A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017378



Internal ID19106595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69987711..70015126hg38UCSC Ensembl
Innerchr8:70899946..70927361hg19UCSC Ensembl
Innerchr8:71062500..71089915hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3827416
hg1927416
hg1827416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689512, nssv3689511
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)nsv1017378
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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