A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120015



Internal ID18912270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85739639..85739957hg38UCSC Ensembl
Outerchr4:86660792..86661110hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2843n106
Supporting Variantsnssv3983035
SamplesKWS1
Known GenesARHGAP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120015
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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