A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950981



Internal ID16953168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:79298144..79315643hg38UCSC Ensembl
Outerchr10:81057901..81075400hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3817500
hg1917500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998013
SamplesBILGI_BIOE
Known GenesZMIZ1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950981
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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