A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951129



Internal ID17300003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39373982..39529581hg38UCSC Ensembl
Outerchr8:39231501..39387100hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155600
hg19155600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999255
SamplesBILGI_BIOE
Known GenesADAM3A, ADAM5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951129
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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