A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015437



Internal ID19104654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8823745..8866288hg38UCSC Ensembl
Innerchr8:8681255..8723798hg19UCSC Ensembl
Innerchr8:8718665..8761208hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3842544
hg1942544
hg1842544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681690
Samples
Known GenesMFHAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015437
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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