A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950991



Internal ID17299865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:88832744..88854143hg38UCSC Ensembl
Outerchr10:90592501..90613900hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3821400
hg1921400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998023
SamplesBILGI_BIOE
Known GenesANKRD22
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950991
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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