A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143290



Internal ID18907994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85696152..85696252hg38UCSC Ensembl
Outerchr4:86617305..86617405hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980474
SamplesKWS1
Known GenesARHGAP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143290
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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