A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026582



Internal ID19115800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40326266..40338108hg38UCSC Ensembl
Innerchr8:40183785..40195627hg19UCSC Ensembl
Innerchr8:40302942..40314784hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3811843
hg1911843
hg1811843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7183n100
Supporting Variantsnssv3687226, nssv3687219, nssv3757229, nssv3757227, nssv3687232, nssv3687229, nssv3687220, nssv3687225, nssv3687222, nssv3687221, nssv3687233, nssv3687230, nssv3687227, nssv3687231, nssv3687224, nssv3757228, nssv3687223, nssv3687228
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)nsv1026582
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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