A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142403



Internal ID19258882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:105629589..105653600hg38UCSC Ensembl
Outerchr4:106550746..106574757hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3824012
hg1924012
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993908
SamplesKWS2
Known GenesARHGEF38
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142403
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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