A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111645



Internal ID18903619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85739632..85739931hg38UCSC Ensembl
Outerchr4:86660785..86661084hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2843n106
Supporting Variantsnssv3964541
SamplesKWS2
Known GenesARHGAP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111645
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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