A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073315



Internal ID19316485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26388031..26391027hg38UCSC Ensembl
chr4:26389653..26392649hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382997
hg192997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768424
SamplesKWP1
Known GenesRBPJ
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073315
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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