A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649133



Internal ID18600728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172653521..172732234hg38UCSC Ensembl
Innerchr5:172080524..172159237hg19UCSC Ensembl
Innerchr5:172013129..172091842hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3878714
hg1978714
hg1878714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018207
Supporting Variants
Samples
Known GenesNEURL1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649133
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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