A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033547



Internal ID18776080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38996094..39315027hg38UCSC Ensembl
Innerchr9:38996091..39315024hg19UCSC Ensembl
Innerchr9:38986091..39305024hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38318934
hg19318934
hg18318934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7525n100
Supporting Variantsnssv3688928
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033547
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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