A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687239



Internal ID18985520
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 StatusS
Merged Variantsnsv1020746
Supporting Variants
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)nssv3687239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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