A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950004



Internal ID16952191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:142733583..142811684hg38UCSC Ensembl
Outerchr8:143815001..143893100hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3878102
hg1978100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999343
SamplesBILGI_BIOE
Known GenesLY6D, LYNX1, LYPD2, SLURP1, THEM6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950004
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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