A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975063



Internal ID18610271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55594691..55600744hg38UCSC Ensembl
Innerchr10:57354451..57360504hg19UCSC Ensembl
Innerchr10:57024457..57030510hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg386054
hg196054
hg186054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759163
SamplesHGDP01284
Known GenesMTRNR2L5
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975063
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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