A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977745



Internal ID18897906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:57340802..57420102hg38UCSC Ensembl
Outerchr6:57205600..57284900hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3879301
hg1979301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124939
Supporting Variants
SamplesKWS2
Known GenesPRIM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977745
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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