A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958245



Internal ID17307118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91209458..91209794hg38UCSC Ensembl
Outerchr10:92969215..92969551hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001985
SamplesBILGI_BIOE
Known GenesPCGF5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958245
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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