A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951126



Internal ID16953313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:37827983..37845682hg38UCSC Ensembl
Outerchr8:37685501..37703200hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3817700
hg1917700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999252
SamplesBILGI_BIOE
Known GenesBRF2, GPR124
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951126
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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