A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951888



Internal ID17300762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132290297..132294696hg38UCSC Ensembl
Outerchr10:134103801..134108200hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998085
SamplesBILGI_BIOE
Known GenesSTK32C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951888
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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