A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151095



Internal ID19201001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:869615..869689hg38UCSC Ensembl
Outerchr4:863403..863477hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002031
SamplesKWB1
Known GenesGAK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151095
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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