A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977758



Internal ID18612964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96448104..96448820hg38UCSC Ensembl
Innerchr15:96991334..96992050hg19UCSC Ensembl
Innerchr15:94792338..94793054hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38717
hg19717
hg18717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2037918, nssv2037919, nssv2037916, nssv2037917, nssv2037920, nssv2037921, nssv2037913, nssv2037922, nssv2037914, nssv2037915
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)nsv977758
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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