A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963359



Internal ID18869138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:7741539..7741621hg38UCSC Ensembl
Outerchr5:7741652..7741734hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111292
Supporting Variants
SamplesKWS1
Known GenesADCY2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963359
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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