A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974557



Internal ID18263082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34509908..34557463hg38UCSC Ensembl
Innerchr15:34802109..34849664hg19UCSC Ensembl
Innerchr15:32589401..32636956hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3847556
hg1947556
hg1847556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2017207, nssv2017214, nssv2017212, nssv2017211, nssv2017213, nssv2017209, nssv2017216, nssv2017215, nssv2017210, nssv2017208
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974557
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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