A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005260



Internal ID16951526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85875245..85875409hg38UCSC Ensembl
Outerchr4:86796398..86796562hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956400
Supporting Variants
SamplesBILGI_BIOE
Known GenesARHGAP24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005260
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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