A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044064



Internal ID18786595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69483640..69505192hg38UCSC Ensembl
Innerchr9:72098556..72120108hg19UCSC Ensembl
Innerchr9:71288376..71309928hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821553
hg1921553
hg1821553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7673n100
Supporting Variantsnssv3696313
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)nsv1044064
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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