A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022917



Internal ID19112134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12407033..12513862hg38UCSC Ensembl
Innerchr8:12264542..12371371hg19UCSC Ensembl
Innerchr8:12308913..12415742hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38106830
hg19106830
hg18106830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7069n100
Supporting Variantsnssv3666898, nssv3666897
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)nsv1022917
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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