A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026714



Internal ID19115932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85588026..85638777hg38UCSC Ensembl
Innerchr8:86500255..86551006hg19UCSC Ensembl
Innerchr8:86687507..86738258hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3850752
hg1950752
hg1850752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7256n100
Supporting Variantsnssv3689654
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)nsv1026714
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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