A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026507



Internal ID19115725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85603620..85645172hg38UCSC Ensembl
Innerchr8:86515849..86557401hg19UCSC Ensembl
Innerchr8:86703101..86744653hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3841553
hg1941553
hg1841553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7258n100
Supporting Variantsnssv3689659, nssv3757310, nssv3689660
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)nsv1026507
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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