A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977722



Internal ID18612928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59767192..59771132hg38UCSC Ensembl
Innerchr15:60059391..60063331hg19UCSC Ensembl
Innerchr15:57846683..57850623hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383941
hg193941
hg183941
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2027335, nssv2027342, nssv2027340, nssv2027337, nssv2027338, nssv2027344, nssv2027341, nssv2027339, nssv2027343, nssv2027336
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)nsv977722
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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