A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132631



Internal ID19272648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160634568..160646768hg38UCSC Ensembl
Outerchr6:161055600..161067800hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3812201
hg1912201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3427n106
Supporting Variantsnssv3987418
SamplesKWS1
Known GenesLPA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132631
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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