A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977698



Internal ID18612904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34849955..34850742hg38UCSC Ensembl
Innerchr15:35142156..35142943hg19UCSC Ensembl
Innerchr15:32929448..32930235hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38788
hg19788
hg18788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2017724, nssv2017720, nssv2017723, nssv2017716, nssv2017717, nssv2017718, nssv2017721, nssv2017719, nssv2017725, nssv2017722
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)nsv977698
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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