A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961000



Internal ID18864322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:52244737..52244822hg38UCSC Ensembl
Outerchr10:54004497..54004582hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120221
Supporting Variants
SamplesKWS1
Known GenesPRKG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961000
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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