A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975799



Internal ID18264320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48894013..48898411hg38UCSC Ensembl
Innerchr10:50102058..50106456hg19UCSC Ensembl
Innerchr10:49772064..49776462hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg384399
hg194399
hg184399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763042
SamplesHGDP00998
Known GenesWDFY4
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975799
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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