A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976927



Internal ID18612133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42570750..42576245hg38UCSC Ensembl
Innerchr15:42862948..42868443hg19UCSC Ensembl
Innerchr15:40650240..40655735hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg385496
hg195496
hg185496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2019630, nssv2019632, nssv2019634, nssv2019637, nssv2019636, nssv2019631, nssv2019628, nssv2019629, nssv2019635, nssv2019633
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSTARD9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976927
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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