A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950960



Internal ID16953147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45876167..45959835hg38UCSC Ensembl
Outerchr10:51636001..51723000hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3883669
hg1987000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997992
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950960
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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