A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023001



Internal ID19112218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36559791..36624593hg38UCSC Ensembl
Innerchr8:36417309..36482111hg19UCSC Ensembl
Innerchr8:36536467..36601269hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3864803
hg1964803
hg1864803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7161n100
Supporting Variantsnssv3760500
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)nsv1023001
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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