A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031415



Internal ID19120637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40326266..40336937hg38UCSC Ensembl
Innerchr8:40183785..40194456hg19UCSC Ensembl
Innerchr8:40302942..40313613hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810672
hg1910672
hg1810672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7183n100
Supporting Variantsnssv3687215, nssv3687216, nssv3687214, nssv3687217, nssv3687213, nssv3687212, nssv3687218
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)nsv1031415
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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