A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980188



Internal ID18268702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25713016..25721336hg38UCSC Ensembl
Innerchr4:25714638..25722958hg19UCSC Ensembl
Innerchr4:25323736..25332056hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388321
hg198321
hg188321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2315286, nssv2315281, nssv2315284, nssv2315280, nssv2315289, nssv2315283, nssv2315282, nssv2315287, nssv2315288, nssv2315285
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)nsv980188
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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