A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984088



Internal ID19235994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:75610906..75610995hg38UCSC Ensembl
Outerchr6:76320622..76320711hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125881
Supporting Variants
SamplesKWS2
Known GenesSENP6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984088
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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