A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964092



Internal ID18872579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:69920974..69921069hg38UCSC Ensembl
Outerchr6:70630866..70630961hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129760
Supporting Variants
SamplesKWS1
Known GenesCOL19A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964092
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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