A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966341



Internal ID18254885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173615444..173634324hg38UCSC Ensembl
Innerchr4:174536595..174555475hg19UCSC Ensembl
Innerchr4:174773170..174792050hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3818881
hg1918881
hg1818881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2341090, nssv2341085, nssv2341089, nssv2341084, nssv2341092, nssv2341091, nssv2341087, nssv2341088, nssv2341083, nssv2341086
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)nsv966341
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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