A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023890



Internal ID18766423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39053783..39330072hg38UCSC Ensembl
Innerchr9:39053780..39330069hg19UCSC Ensembl
Innerchr9:39043780..39320069hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38276290
hg19276290
hg18276290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7530n100
Supporting Variantsnssv3688936
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)nsv1023890
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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