A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977699



Internal ID18612905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34941924..34943980hg38UCSC Ensembl
Innerchr15:35234125..35236181hg19UCSC Ensembl
Innerchr15:33021417..33023473hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382057
hg192057
hg182057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2018607, nssv2018608, nssv2018609, nssv2018610, nssv2018605, nssv2018611, nssv2018612, nssv2018613, nssv2018614, nssv2018606
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAQR
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977699
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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