A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035814



Internal ID18778345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69475890..69505349hg38UCSC Ensembl
Innerchr9:72090806..72120265hg19UCSC Ensembl
Innerchr9:71280626..71310085hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3829460
hg1929460
hg1829460
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696249, nssv3696250, nssv3696251
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035814
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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