A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019595



Internal ID18762130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12176786..12709141hg38UCSC Ensembl
Innerchr8:12034295..12566650hg19UCSC Ensembl
Innerchr8:12071704..12611021hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38532356
hg19532356
hg18539318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7016n100
Supporting Variantsnssv3754353
Samples
Known GenesDEFB109P1, DEFB130, FAM66A, FAM86B1, FAM86B2, FAM90A25P, FAM90A2P, LOC100133267, LOC100506990, LOC649352, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019595
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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