A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034355



Internal ID19123577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40084660..40103913hg38UCSC Ensembl
Innerchr8:39942179..39961432hg19UCSC Ensembl
Innerchr8:40061336..40080589hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3819254
hg1919254
hg1819254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687210
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)nsv1034355
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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