A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026923



Internal ID19116141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12446591..12532643hg38UCSC Ensembl
Innerchr8:12304100..12390152hg19UCSC Ensembl
Innerchr8:12348471..12434523hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3886053
hg1986053
hg1886053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7072n100
Supporting Variantsnssv3666916
Samples
Known GenesLOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026923
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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