A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146862



Internal ID19196065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160532505..160538057hg38UCSC Ensembl
Outerchr6:160953537..160959089hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385553
hg195553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998226
SamplesKWB1
Known GenesLPA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146862
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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