A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027737



Internal ID19116955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12562779hg38UCSC Ensembl
Innerchr8:12260915..12420288hg19UCSC Ensembl
Innerchr8:12305286..12464659hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38159374
hg19159374
hg18159374
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7070n100
Supporting Variantsnssv3665978, nssv3665977, nssv3665976, nssv3665973, nssv3760141, nssv3665979, nssv3665975, nssv3665974
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027737
Frequency
Sample Size11257
Observed Gain2
Observed Loss6
Observed Complex0
Frequencyn/a


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