A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132626



Internal ID18905717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:57436802..60345251hg38UCSC Ensembl
Outerchr6:57301600..57317100hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg382908450
hg1915501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3323n106
Supporting Variantsnssv3987412
SamplesKWS1
Known GenesPRIM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132626
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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