A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015872



Internal ID18758406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38796098..39330072hg38UCSC Ensembl
Innerchr9:38796095..39330069hg19UCSC Ensembl
Innerchr9:38786095..39320069hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38533975
hg19533975
hg18533975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688896, nssv3688897, nssv3688895
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)nsv1015872
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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