A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025365



Internal ID18767897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121311006..121382534hg38UCSC Ensembl
Innerchr8:122323246..122394774hg19UCSC Ensembl
Innerchr8:122392427..122463955hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3871529
hg1971529
hg1871529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757363, nssv3691480
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025365
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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