A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993031



Internal ID19227901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170091376..170098676hg38UCSC Ensembl
Outerchr6:170406600..170413900hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg387301
hg197301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141524
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993031
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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