A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962128



Internal ID18876640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:180249524..180249620hg38UCSC Ensembl
Outerchr5:179676524..179676620hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125864
Supporting Variants
SamplesKWS1
Known GenesMAPK9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962128
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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