A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763977



Internal ID19311642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:33034459..33034510hg38UCSC Ensembl
Outerchr4:33036081..33036132hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078813
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763977
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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