A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045508



Internal ID18788039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109873706..110035007hg38UCSC Ensembl
Innerchr9:112635986..112797287hg19UCSC Ensembl
Innerchr9:111675807..111837108hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38161302
hg19161302
hg18161302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695043
Samples
Known GenesPALM2, PALM2-AKAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045508
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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