A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963038



Internal ID18598280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34227132..34228341hg38UCSC Ensembl
Innerchr19:34718037..34719246hg19UCSC Ensembl
Innerchr19:39409877..39411086hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381210
hg191210
hg181210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2145133, nssv2145127, nssv2145134, nssv2145135, nssv2145128, nssv2145126, nssv2145130, nssv2145132, nssv2145131, nssv2145129
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLSM14A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963038
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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