A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961066



Internal ID18863731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:124357763..124357846hg38UCSC Ensembl
Outerchr12:124842309..124842392hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120270
Supporting Variants
SamplesKWS1
Known GenesNCOR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961066
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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