A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998741



Internal ID18847816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2649860..2702761hg38UCSC Ensembl
Outerchr1:2581299..2634200hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3852902
hg1952902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149955
Supporting Variants
SamplesKWB1
Known GenesTTC34
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998741
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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