A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138779



Internal ID18912004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:163322927..163323000hg38UCSC Ensembl
Outerchr6:163743959..163744032hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3434n106
Supporting Variantsnssv3991372
SamplesKWS1
Known GenesPACRG-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138779
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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