A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145829



Internal ID18854041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85696135..85696243hg38UCSC Ensembl
Outerchr4:86617288..86617396hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997193
SamplesKWB1
Known GenesARHGAP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145829
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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