A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028234



Internal ID19117452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61587481hg38UCSC Ensembl
Innerchr9:44727847..44795319hg19UCSC Ensembl
Innerchr9:44667843..44735315hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3867473
hg1967473
hg1867473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691941, nssv3691942
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)nsv1028234
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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