A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020746



Internal ID19109964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40326617..40336937hg38UCSC Ensembl
Innerchr8:40184136..40194456hg19UCSC Ensembl
Innerchr8:40303293..40313613hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810321
hg1910321
hg1810321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7183n100
Supporting Variantsnssv3687239
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)nsv1020746
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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