A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983685



Internal ID18880172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103322408..103322488hg38UCSC Ensembl
Outerchr10:105082165..105082245hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125509
Supporting Variants
SamplesKWS2
Known GenesPCGF6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983685
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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