A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153921



Internal ID18853655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:142840301..142840396hg38UCSC Ensembl
Outerchr6:143161438..143161533hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003197
SamplesKWB1
Known GenesHIVEP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153921
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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