A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140195



Internal ID18908398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:105286821..105286898hg38UCSC Ensembl
Outerchr6:105734696..105734773hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978907
SamplesKWS2
Known GenesPREP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140195
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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