A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001422



Internal ID18841625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:101736264..101736349hg38UCSC Ensembl
Outerchr10:103496021..103496106hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153506
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001422
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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