A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136884



Internal ID18914559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85874758..85874814hg38UCSC Ensembl
Outerchr4:86795911..86795967hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974792, nssv3956748
SamplesKWS1, KWS2
Known GenesARHGAP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136884
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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