A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977760



Internal ID18612966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99276882..99285851hg38UCSC Ensembl
Innerchr15:99817087..99826056hg19UCSC Ensembl
Innerchr15:97634610..97643579hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg388970
hg198970
hg188970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2036897, nssv2036895, nssv2036888, nssv2036891, nssv2036890, nssv2036896, nssv2036893, nssv2036892, nssv2036894, nssv2036889
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLRRC28
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977760
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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