A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977726



Internal ID18612932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60557839..60559935hg38UCSC Ensembl
Innerchr15:60850038..60852134hg19UCSC Ensembl
Innerchr15:58637330..58639426hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg382097
hg192097
hg182097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2027039, nssv2027042, nssv2027043, nssv2027044, nssv2027040, nssv2027045, nssv2027046, nssv2027038, nssv2027037, nssv2027041
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRORA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977726
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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