A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041391



Internal ID18783922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69482727..69505192hg38UCSC Ensembl
Innerchr9:72097643..72120108hg19UCSC Ensembl
Innerchr9:71287463..71309928hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3822466
hg1922466
hg1822466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7673n100
Supporting Variantsnssv3696265
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)nsv1041391
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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