A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019959



Internal ID19109178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12384994..12505127hg38UCSC Ensembl
Innerchr8:12242503..12362636hg19UCSC Ensembl
Innerchr8:12286874..12407007hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38120134
hg19120134
hg18120134
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7052n100
Supporting Variantsnssv3664910, nssv3760073, nssv3664908, nssv3664909
Samples
Known GenesDEFB109P1, FAM66A, 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)nsv1019959
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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