A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950762



Internal ID16952949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:3090567..3093866hg38UCSC Ensembl
Outerchr6:3090801..3094100hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997393
SamplesBILGI_BIOE
Known GenesRIPK1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950762
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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