A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564101



Internal ID18515696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10142986..10596015hg38UCSC Ensembl
Innerchr18:10142983..10596012hg19UCSC Ensembl
Innerchr18:10132983..10586012hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38453030
hg19453030
hg18453030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059110
Supporting Variants
Samples
Known GenesAPCDD1, NAPG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564101
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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