A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956518



Internal ID17305391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:28222383..28222754hg38UCSC Ensembl
Outerchr6:28190161..28190532hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003427
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956518
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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