A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074253



Internal ID19320869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186292786..186293584hg38UCSC Ensembl
chr4:187213940..187214738hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769203
SamplesKWP1
Known GenesF11-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074253
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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