A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151176



Internal ID19195759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:6932336..6932481hg38UCSC Ensembl
Outerchr6:6932569..6932714hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002113
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151176
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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