A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976958



Internal ID18265478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82539133..82540764hg38UCSC Ensembl
Innerchr15:82823541..82825172hg19UCSC Ensembl
Innerchr15:80610596..80612227hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381632
hg191632
hg181632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2035026, nssv2035030, nssv2035029, nssv2035032, nssv2035033, nssv2035031, nssv2035025, nssv2035028, nssv2035024, nssv2035027
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesRPS17, RPS17L
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976958
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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