A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977725



Internal ID18612931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60403721..60406670hg38UCSC Ensembl
Innerchr15:60695920..60698869hg19UCSC Ensembl
Innerchr15:58483212..58486161hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg382950
hg192950
hg182950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028516, nssv2028524, nssv2028515, nssv2028521, nssv2028519, nssv2028522, nssv2028520, nssv2028517, nssv2028518, nssv2028523
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)nsv977725
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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