A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6034n71



Internal ID6323654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35850693..35861068hg19UCSC Ensembl
chr5:35886450..35896825hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv881358, nsv881685, nsv881055
SamplesSP51058, SP54726, SP54406, SP50691, SP50046, SP80936, SP57925, SP52055, SP56861, SP58305, SP56880, SP56874, SP52559, SP57553, SP52688, SP55926
Known GenesIL7R
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6034n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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