A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129273



Internal ID18923932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160728225..160728290hg38UCSC Ensembl
Outerchr6:161149257..161149322hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962706
SamplesKWS1
Known GenesPLG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129273
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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