A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078529



Internal ID18979720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13299..68808hg38UCSC Ensembl
chr4:13299..68700hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3855510
hg1955402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766957
SamplesKWP1
Known GenesZNF595, ZNF718
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078529
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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