A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950158



Internal ID16952345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:33678024..33695723hg38UCSC Ensembl
Outerchr6:33645801..33663500hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3817700
hg1917700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997430
SamplesBILGI_BIOE
Known GenesITPR3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950158
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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