A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976954



Internal ID18612160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77861004..77963483hg38UCSC Ensembl
Innerchr15:78153346..78255825hg19UCSC Ensembl
Innerchr15:75940401..76042880hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38102480
hg19102480
hg18102480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2033895, nssv2033893, nssv2033901, nssv2033894, nssv2033902, nssv2033897, nssv2033899, nssv2033898, nssv2033900, nssv2033896
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC645752
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976954
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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