A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073781



Internal ID18977406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85739663..85740045hg38UCSC Ensembl
chr4:86660816..86661198hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771682
SamplesKWP1
Known GenesARHGAP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073781
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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