A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127861



Internal ID18912489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:163322924..163323008hg38UCSC Ensembl
Outerchr6:163743956..163744040hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3434n106
Supporting Variantsnssv3956465
SamplesKWS1
Known GenesPACRG-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127861
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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