A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997795



Internal ID19157332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:125816644..125877966hg38UCSC Ensembl
Innerchr4:126737799..126799121hg19UCSC Ensembl
Innerchr4:126957249..127018571hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3861323
hg1961323
hg1861323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5383n100
Supporting Variantsnssv3639418
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)nsv997795
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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