A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984044



Internal ID18619234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30822225..30834344hg38UCSC Ensembl
Innerchr15:31114428..31126547hg19UCSC Ensembl
Innerchr15:28901720..28913839hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3812120
hg1912120
hg1812120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2015768, nssv2015764, nssv2015765, nssv2015759, nssv2015761, nssv2015766, nssv2015767, nssv2015760, nssv2015762, nssv2015763
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984044
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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