A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029604



Internal ID18772135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12142788..12545643hg38UCSC Ensembl
Innerchr8:12000297..12403152hg19UCSC Ensembl
Innerchr8:12037706..12447523hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38402856
hg19402856
hg18409818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7025n100
Supporting Variantsnssv3681901
Samples
Known GenesDEFB109P1, DEFB130, FAM66A, FAM66D, 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)nsv1029604
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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