A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956422



Internal ID16958609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85695950..85696099hg38UCSC Ensembl
Outerchr4:86617103..86617252hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005316
SamplesBILGI_BIOE
Known GenesARHGAP24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956422
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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