A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950014



Internal ID16952201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:143786431..143842128hg38UCSC Ensembl
Outerchr8:144868601..144924300hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3855698
hg1955700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999352
SamplesBILGI_BIOE
Known GenesMIR6845, MIR937, NRBP2, PUF60, SCRIB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950014
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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