A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951886



Internal ID16954073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132219797..132258596hg38UCSC Ensembl
Outerchr10:134033301..134072100hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3838800
hg1938800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998083
SamplesBILGI_BIOE
Known GenesSTK32C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951886
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer