A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964122



Internal ID18599360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184908397..184920781hg38UCSC Ensembl
Innerchr4:185829551..185841935hg19UCSC Ensembl
Innerchr4:186066545..186078929hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3812385
hg1912385
hg1812385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2343566, nssv2343564, nssv2343572, nssv2343565, nssv2343569, nssv2343563, nssv2343570, nssv2343571, nssv2343567, nssv2343568
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964122
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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