A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032173



Internal ID19121395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12406228..12486092hg38UCSC Ensembl
Innerchr8:12263737..12343601hg19UCSC Ensembl
Innerchr8:12308108..12387972hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3879865
hg1979865
hg1879865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3666888
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032173
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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