A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975797



Internal ID18264318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37594193..37615719hg38UCSC Ensembl
Innerchr10:37883121..37904647hg19UCSC Ensembl
Innerchr10:37923127..37944653hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3821527
hg1921527
hg1821527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759194, nssv2758463
SamplesHGDP00778, HGDP00998
Known GenesMTRNR2L7
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975797
Frequency
Sample Size10
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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