A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950773



Internal ID16952960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:15248170..15248769hg38UCSC Ensembl
Outerchr6:15248401..15249000hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997403
SamplesBILGI_BIOE
Known GenesJARID2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950773
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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