A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642100



Internal ID18940381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50265382hg38UCSC Ensembl
Innerchr5:49455624..49561216hg19UCSC Ensembl
Innerchr5:49491381..49596973hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38105593
hg19105593
hg18105593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025722
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642100
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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