A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964088



Internal ID19205326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:27346037..27346105hg38UCSC Ensembl
Outerchr6:27313816..27313884hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129758
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964088
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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