A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951234



Internal ID16953421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1540506..1543105hg38UCSC Ensembl
Outerchr10:1582701..1585300hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997070
SamplesBILGI_BIOE
Known GenesADARB2, ADARB2-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951234
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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