A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971641



Internal ID18606858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36322625..36324858hg38UCSC Ensembl
Innerchr8:36180143..36182376hg19UCSC Ensembl
Innerchr8:36299688..36301924hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382234
hg192234
hg182237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2499414, nssv2499416, nssv2499409, nssv2499411, nssv2499412, nssv2499415, nssv2499417, nssv2499413, nssv2499410, nssv2499418
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)nsv971641
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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