A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974577



Internal ID18609788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52884572..52891259hg38UCSC Ensembl
Innerchr15:53176769..53183456hg19UCSC Ensembl
Innerchr15:50964061..50970748hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386688
hg196688
hg186688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2024386, nssv2024388, nssv2024387, nssv2024381, nssv2024382, nssv2024383, nssv2024379, nssv2024385, nssv2024384, nssv2024380
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)nsv974577
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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